Canonical Allele Identifier: CA430903635
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203329638G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464915G>T , CM000664.2:g.202464915G>T GRCh38
NC_000002.11:g.203329638G>T , CM000664.1:g.203329638G>T GRCh37
NC_000002.10:g.203037883G>T NCBI36
NG_009363.1:g.93589G>T , LRG_712:g.93589G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.183G>T MANE Select ENSP00000363708.4:p.Ser61=
ENST00000638587.1:c.108G>T ENSP00000491062.1:p.Ser36=
ENST00000374574.2:c.183G>T ENSP00000363702.2:p.Ser61=
ENST00000374580.8:c.183G>T ENSP00000363708.4:p.Ser61=
ENST00000479069.1:n.90G>T
NM_001204.6:c.183G>T , LRG_712t1:c.183G>T NP_001195.2:p.Ser61=
XM_011511687.1:c.183G>T XP_011509989.1:p.Ser61=
XM_011511688.1:c.183G>T XP_011509990.1:p.Ser61=
NM_001204.7:c.183G>T MANE Select NP_001195.2:p.Ser61=