Canonical Allele Identifier: CA763418184
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1207554352
MyVariant Identifiers: chr2:g.203241189C>A (hg19) chr2:g.202376466C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202376466C>A , CM000664.2:g.202376466C>A GRCh38
NC_000002.11:g.203241189C>A , CM000664.1:g.203241189C>A GRCh37
NC_000002.10:g.202949434C>A NCBI36
NG_009363.1:g.5140C>A , LRG_712:g.5140C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.-1009C>A MANE Select ENSP00000363708.4:n.-1009C>A
NM_001204.6:c.-1009C>A , LRG_712t1:c.-1009C>A NP_001195.2:n.-1009C>A
XM_011511687.1:c.-1009C>A XP_011509989.1:n.-1009C>A
XM_011511688.1:c.-1009C>A XP_011509990.1:n.-1009C>A
NM_001204.7:c.-1009C>A MANE Select NP_001195.2:n.-1009C>A
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