Canonical Allele Identifier: CA763418065
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1202867149
MyVariant Identifiers: chr2:g.203241042G>C (hg19) chr2:g.202376319G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202376319G>C , CM000664.2:g.202376319G>C GRCh38
NC_000002.11:g.203241042G>C , CM000664.1:g.203241042G>C GRCh37
NC_000002.10:g.202949287G>C NCBI36
NG_009363.1:g.4993G>C , LRG_712:g.4993G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011511687.1:c.-1156G>C XP_011509989.1:n.-1156G>C
XM_011511688.1:c.-1156G>C XP_011509990.1:n.-1156G>C
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