Canonical Allele Identifier: CA16397117
Gene: BMPR1A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11202221

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86842557T>G , CM000672.2:g.86842557T>G GRCh38
NC_000010.10:g.88602314T>G , CM000672.1:g.88602314T>G GRCh37
NC_000010.9:g.88592294T>G NCBI36
NG_009362.1:g.90919T>G , LRG_298:g.90919T>G

Transcript Alleles

HGVS Amino-acid change
NM_004329.2:c.-153+3578T>G , LRG_298t1:c.-153+3578T>G NP_004320.2:p.=
XM_011540103.1:c.-153+3578T>G XP_011538405.1:p.=
XM_011540104.1:c.-257-849T>G XP_011538406.1:p.=
XM_011540103.2:c.-153+3578T>G
XM_011540104.2:c.-257-849T>G
ENST00000372037.7:c.-153+3578T>G ENSP00000361107.1:p.=
ENST00000480152.2:c.-257-849T>G ENSP00000483569.1:p.=