Canonical Allele Identifier: CA64029570

Gene: BMPR2

Linked Data

• dbSNP Id: rs1046458343
• gnomAD v4: 2-202532719-A-G
• MyVariant Identifiers: chr2:g.203397442A>G (hg19) ; chr2:g.202532719A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202532719A>G , CM000664.2:g.202532719A>G	GRCh38
NC_000002.11:g.203397442A>G , CM000664.1:g.203397442A>G	GRCh37
NC_000002.10:g.203105687A>G	NCBI36
NG_009363.1:g.161393A>G , LRG_712:g.161393A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374580.10:c.1263A>G MANE Select	ENSP00000363708.4:p.Thr421=
ENST00000638587.1:c.1194A>G	ENSP00000491062.1:p.Thr398=
ENST00000374574.2:c.1263A>G	ENSP00000363702.2:p.Thr421=
ENST00000374580.8:c.1263A>G	ENSP00000363708.4:p.Thr421=
NM_001204.6:c.1263A>G , LRG_712t1:c.1263A>G	NP_001195.2:p.Thr421=
XM_011511687.1:c.1263A>G	XP_011509989.1:p.Thr421=
XM_011511688.1:c.1263A>G	XP_011509990.1:p.Thr421=
NM_001204.7:c.1263A>G MANE Select	NP_001195.2:p.Thr421=