Canonical Allele Identifier: CA1477875581
Gene: BMPR1B HGNC NCBI

Linked Data

dbSNP Id: rs1729251792

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935380C>A , CM000666.2:g.94935380C>A GRCh38
NC_000004.11:g.95856531C>A , CM000666.1:g.95856531C>A GRCh37
NC_000004.10:g.96075554C>A NCBI36
NG_009245.1:g.182404C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59480C>A MANE Select ENSP00000426617.1:n.-113+59480C>A
ENST00000515059.5:c.-113+59480C>A ENSP00000426617.1:n.-113+59480C>A
NM_001203.2:c.-113+59480C>A NP_001194.1:n.-113+59480C>A
XM_011532201.1:c.-18+59480C>A XP_011530503.1:n.-18+59480C>A
XM_011532201.2:c.-18+59480C>A XP_011530503.1:n.-18+59480C>A
XM_017008558.1:c.-113+59480C>A XP_016864047.1:n.-113+59480C>A
XM_017008559.1:c.-113+36330C>A XP_016864048.1:n.-113+36330C>A
NM_001203.3:c.-113+59480C>A MANE Select NP_001194.1:n.-113+59480C>A