Canonical Allele Identifier: CA350349139
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203421017G>C (hg19) chr2:g.202556294G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556294G>C , CM000664.2:g.202556294G>C GRCh38
NC_000002.11:g.203421017G>C , CM000664.1:g.203421017G>C GRCh37
NC_000002.10:g.203129262G>C NCBI36
NG_009363.1:g.184968G>C , LRG_712:g.184968G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.2629G>C MANE Select ENSP00000363708.4:p.Ala877Pro
ENST00000638587.1:c.2560G>C ENSP00000491062.1:n.2560G>C
ENST00000374574.2:c.1587-3402G>C ENSP00000363702.2:n.1587-3402G>C
ENST00000374580.8:c.2629G>C ENSP00000363708.4:p.Ala877Pro
NM_001204.6:c.2629G>C , LRG_712t1:c.2629G>C NP_001195.2:p.Ala877Pro
XM_011511687.1:c.2629G>C XP_011509989.1:p.Ala877Pro
XM_011511688.1:c.1587-3402G>C XP_011509990.1:n.1587-3402G>C
NM_001204.7:c.2629G>C MANE Select NP_001195.2:p.Ala877Pro
Search 100 bp 5'
Search 100 bp 3'