Canonical Allele Identifier: CA430838932
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs750524280
MyVariant Identifiers: chr2:g.203383583C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202518860C>T , CM000664.2:g.202518860C>T GRCh38
NC_000002.11:g.203383583C>T , CM000664.1:g.203383583C>T GRCh37
NC_000002.10:g.203091828C>T NCBI36
NG_009363.1:g.147534C>T , LRG_712:g.147534C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.660C>T MANE Select ENSP00000363708.4:p.Gly220=
ENST00000638587.1:c.591C>T ENSP00000491062.1:p.Gly197=
ENST00000374574.2:c.660C>T ENSP00000363702.2:p.Gly220=
ENST00000374580.8:c.660C>T ENSP00000363708.4:p.Gly220=
NM_001204.6:c.660C>T , LRG_712t1:c.660C>T NP_001195.2:p.Gly220=
XM_011511687.1:c.660C>T XP_011509989.1:p.Gly220=
XM_011511688.1:c.660C>T XP_011509990.1:p.Gly220=
NM_001204.7:c.660C>T MANE Select NP_001195.2:p.Gly220=