Canonical Allele Identifier: CA430859522
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203417444G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552721G>T , CM000664.2:g.202552721G>T GRCh38
NC_000002.11:g.203417444G>T , CM000664.1:g.203417444G>T GRCh37
NC_000002.10:g.203125689G>T NCBI36
NG_009363.1:g.181395G>T , LRG_712:g.181395G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1419G>T MANE Select ENSP00000363708.4:p.Val473=
ENST00000638587.1:c.1350G>T ENSP00000491062.1:p.Val450=
ENST00000374574.2:c.1419G>T ENSP00000363702.2:p.Val473=
ENST00000374580.8:c.1419G>T ENSP00000363708.4:p.Val473=
NM_001204.6:c.1419G>T , LRG_712t1:c.1419G>T NP_001195.2:p.Val473=
XM_011511687.1:c.1419G>T XP_011509989.1:p.Val473=
XM_011511688.1:c.1419G>T XP_011509990.1:p.Val473=
NM_001204.7:c.1419G>T MANE Select NP_001195.2:p.Val473=