Canonical Allele Identifier: CA430859805
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203417504T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552781T>C , CM000664.2:g.202552781T>C GRCh38
NC_000002.11:g.203417504T>C , CM000664.1:g.203417504T>C GRCh37
NC_000002.10:g.203125749T>C NCBI36
NG_009363.1:g.181455T>C , LRG_712:g.181455T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1479T>C MANE Select ENSP00000363708.4:p.Thr493=
ENST00000638587.1:c.1410T>C ENSP00000491062.1:p.Thr470=
ENST00000374574.2:c.1479T>C ENSP00000363702.2:p.Thr493=
ENST00000374580.8:c.1479T>C ENSP00000363708.4:p.Thr493=
NM_001204.6:c.1479T>C , LRG_712t1:c.1479T>C NP_001195.2:p.Thr493=
XM_011511687.1:c.1479T>C XP_011509989.1:p.Thr493=
XM_011511688.1:c.1479T>C XP_011509990.1:p.Thr493=
NM_001204.7:c.1479T>C MANE Select NP_001195.2:p.Thr493=