Canonical Allele Identifier: CA350341509
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1688012022
MyVariant Identifiers: chr2:g.203395628G>T (hg19) chr2:g.202530905G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530905G>T , CM000664.2:g.202530905G>T GRCh38
NC_000002.11:g.203395628G>T , CM000664.1:g.203395628G>T GRCh37
NC_000002.10:g.203103873G>T NCBI36
NG_009363.1:g.159579G>T , LRG_712:g.159579G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1079G>T MANE Select ENSP00000363708.4:p.Gly360Val
ENST00000638587.1:c.1010G>T ENSP00000491062.1:p.Gly337Val
ENST00000374574.2:c.1079G>T ENSP00000363702.2:p.Gly360Val
ENST00000374580.8:c.1079G>T ENSP00000363708.4:p.Gly360Val
NM_001204.6:c.1079G>T , LRG_712t1:c.1079G>T NP_001195.2:p.Gly360Val
XM_011511687.1:c.1079G>T XP_011509989.1:p.Gly360Val
XM_011511688.1:c.1079G>T XP_011509990.1:p.Gly360Val
NM_001204.7:c.1079G>T MANE Select NP_001195.2:p.Gly360Val
Search 100 bp 5'
Search 100 bp 3'