Canonical Allele Identifier: CA763418063
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1253152967
gnomAD v3: 2-202376318-A-G
gnomAD v4: 2-202376318-A-G
MyVariant Identifiers: chr2:g.203241041A>G (hg19) chr2:g.202376318A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202376318A>G , CM000664.2:g.202376318A>G GRCh38
NC_000002.11:g.203241041A>G , CM000664.1:g.203241041A>G GRCh37
NC_000002.10:g.202949286A>G NCBI36
NG_009363.1:g.4992A>G , LRG_712:g.4992A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011511687.1:c.-1157A>G XP_011509989.1:n.-1157A>G
XM_011511688.1:c.-1157A>G XP_011509990.1:n.-1157A>G
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