Canonical Allele Identifier: CA350350288

Gene: BMPR2

Linked Data

• MyVariant Identifiers: chr2:g.203424431C>G (hg19) ; chr2:g.202559708C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202559708C>G , CM000664.2:g.202559708C>G	GRCh38
NC_000002.11:g.203424431C>G , CM000664.1:g.203424431C>G	GRCh37
NC_000002.10:g.203132676C>G	NCBI36
NG_009363.1:g.188382C>G , LRG_712:g.188382C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.2879C>G MANE Select	ENSP00000363708.4:p.Thr960Arg
ENST00000638587.1:c.2810C>G	ENSP00000491062.1:n.2810C>G
ENST00000374574.2:c.*6C>G	ENSP00000363702.2:n.*6C>G
ENST00000374580.8:c.2879C>G	ENSP00000363708.4:p.Thr960Arg
NM_001204.6:c.2879C>G , LRG_712t1:c.2879C>G	NP_001195.2:p.Thr960Arg
XM_011511687.1:c.2876C>G	XP_011509989.1:p.Thr959Arg
XM_011511688.1:c.*6C>G	XP_011509990.1:n.*6C>G
NM_001204.7:c.2879C>G MANE Select	NP_001195.2:p.Thr960Arg