Canonical Allele Identifier: CA350399619
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203332291T>A (hg19) chr2:g.202467568T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467568T>A , CM000664.2:g.202467568T>A GRCh38
NC_000002.11:g.203332291T>A , CM000664.1:g.203332291T>A GRCh37
NC_000002.10:g.203040536T>A NCBI36
NG_009363.1:g.96242T>A , LRG_712:g.96242T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.297T>A MANE Select ENSP00000363708.4:p.Cys99Ter
ENST00000638587.1:c.228T>A ENSP00000491062.1:p.Cys76Ter
ENST00000374574.2:c.297T>A ENSP00000363702.2:p.Cys99Ter
ENST00000374580.8:c.297T>A ENSP00000363708.4:p.Cys99Ter
ENST00000479069.1:n.204T>A
NM_001204.6:c.297T>A , LRG_712t1:c.297T>A NP_001195.2:p.Cys99Ter
XM_011511687.1:c.297T>A XP_011509989.1:p.Cys99Ter
XM_011511688.1:c.297T>A XP_011509990.1:p.Cys99Ter
NM_001204.7:c.297T>A MANE Select NP_001195.2:p.Cys99Ter
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