Canonical Allele Identifier: CA365440505
Gene: ROS1 HGNC NCBI

Linked Data

dbSNP Id: rs2128548497
gnomAD v4: 6-117310213-C-G
MyVariant Identifiers: chr6:g.117631376C>G (hg19) chr6:g.117310213C>G (hg38)
CIViC: CA365440505
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117310213C>G , CM000668.2:g.117310213C>G GRCh38
NC_000006.11:g.117631376C>G , CM000668.1:g.117631376C>G GRCh37
NC_000006.10:g.117738069C>G NCBI36
NG_033929.1:g.120643G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368507.8:c.6284G>C MANE Select ENSP00000357493.3:p.Gly2095Ala
ENST00000368507.7:c.6284G>C ENSP00000357493.3:p.Gly2095Ala
ENST00000368508.7:c.6302G>C ENSP00000357494.3:p.Gly2101Ala
NM_002944.2:c.6302G>C NP_002935.2:p.Gly2101Ala
XM_006715548.2:c.6287G>C XP_006715611.1:p.Gly2096Ala
XM_011536049.1:c.6332G>C XP_011534351.1:p.Gly2111Ala
XM_011536050.1:c.6329G>C XP_011534352.1:p.Gly2110Ala
XM_011536051.1:c.6305G>C XP_011534353.1:p.Gly2102Ala
XM_011536052.1:c.6290G>C XP_011534354.1:p.Gly2097Ala
XM_011536053.1:c.6158G>C XP_011534355.1:p.Gly2053Ala
XM_011536054.1:c.6332G>C XP_011534356.1:p.Gly2111Ala
XM_006715548.4:c.6287G>C XP_006715611.1:p.Gly2096Ala
XM_011536049.2:c.6332G>C XP_011534351.1:p.Gly2111Ala
XM_011536050.2:c.6329G>C XP_011534352.1:p.Gly2110Ala
XM_011536051.2:c.6305G>C XP_011534353.1:p.Gly2102Ala
XM_011536052.2:c.6290G>C XP_011534354.1:p.Gly2097Ala
XM_011536053.2:c.6158G>C XP_011534355.1:p.Gly2053Ala
XM_011536054.2:c.6332G>C XP_011534356.1:p.Gly2111Ala
XM_017011172.1:c.6263G>C XP_016866661.1:p.Gly2088Ala
XM_017011173.1:c.6260G>C XP_016866662.1:p.Gly2087Ala
NM_001378891.1:c.6290G>C NP_001365820.1:p.Gly2097Ala
NM_001378902.1:c.6284G>C MANE Select NP_001365831.1:p.Gly2095Ala
NM_002944.3:c.6302G>C NP_002935.2:p.Gly2101Ala
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