Canonical Allele Identifier: CA430840468
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203384908A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520185A>C , CM000664.2:g.202520185A>C GRCh38
NC_000002.11:g.203384908A>C , CM000664.1:g.203384908A>C GRCh37
NC_000002.10:g.203093153A>C NCBI36
NG_009363.1:g.148859A>C , LRG_712:g.148859A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.951A>C MANE Select ENSP00000363708.4:p.Thr317=
ENST00000638587.1:c.882A>C ENSP00000491062.1:p.Thr294=
ENST00000374574.2:c.951A>C ENSP00000363702.2:p.Thr317=
ENST00000374580.8:c.951A>C ENSP00000363708.4:p.Thr317=
NM_001204.6:c.951A>C , LRG_712t1:c.951A>C NP_001195.2:p.Thr317=
XM_011511687.1:c.951A>C XP_011509989.1:p.Thr317=
XM_011511688.1:c.951A>C XP_011509990.1:p.Thr317=
NM_001204.7:c.951A>C MANE Select NP_001195.2:p.Thr317=