Canonical Allele Identifier: CA350349593
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1356985660

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556408G>A , CM000664.2:g.202556408G>A GRCh38
NC_000002.11:g.203421131G>A , CM000664.1:g.203421131G>A GRCh37
NC_000002.10:g.203129376G>A NCBI36
NG_009363.1:g.185082G>A , LRG_712:g.185082G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2743G>A MANE Select ENSP00000363708.4:p.Val915Ile
ENST00000638587.1:c.2674G>A ENSP00000491062.1:n.2674G>A
ENST00000374574.2:c.1587-3288G>A ENSP00000363702.2:n.1587-3288G>A
ENST00000374580.8:c.2743G>A ENSP00000363708.4:p.Val915Ile
NM_001204.6:c.2743G>A , LRG_712t1:c.2743G>A NP_001195.2:p.Val915Ile
XM_011511687.1:c.2743G>A XP_011509989.1:p.Val915Ile
XM_011511688.1:c.1587-3288G>A XP_011509990.1:n.1587-3288G>A
NM_001204.7:c.2743G>A MANE Select NP_001195.2:p.Val915Ile