Canonical Allele Identifier: CA350399761

Gene: BMPR2

Linked Data

• MyVariant Identifiers: chr2:g.203332356A>T (hg19) ; chr2:g.202467633A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202467633A>T , CM000664.2:g.202467633A>T	GRCh38
NC_000002.11:g.203332356A>T , CM000664.1:g.203332356A>T	GRCh37
NC_000002.10:g.203040601A>T	NCBI36
NG_009363.1:g.96307A>T , LRG_712:g.96307A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374580.10:c.362A>T MANE Select	ENSP00000363708.4:p.Asp121Val
ENST00000638587.1:c.293A>T	ENSP00000491062.1:p.Asp98Val
ENST00000374574.2:c.362A>T	ENSP00000363702.2:p.Asp121Val
ENST00000374580.8:c.362A>T	ENSP00000363708.4:p.Asp121Val
ENST00000479069.1:n.269A>T
NM_001204.6:c.362A>T , LRG_712t1:c.362A>T	NP_001195.2:p.Asp121Val
XM_011511687.1:c.362A>T	XP_011509989.1:p.Asp121Val
XM_011511688.1:c.362A>T	XP_011509990.1:p.Asp121Val
NM_001204.7:c.362A>T MANE Select	NP_001195.2:p.Asp121Val