Canonical Allele Identifier: CA1477970726

Gene: BMPR1B

Linked Data

• dbSNP Id: rs11097457

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95155662A>C , CM000666.2:g.95155662A>C	GRCh38
NC_000004.11:g.96076813A>C , CM000666.1:g.96076813A>C	GRCh37
NC_000004.10:g.96295836A>C	NCBI36
NG_009245.1:g.402686A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000440890.7:c.*989A>C	ENSP00000401907.2:n.*989A>C
ENST00000509540.6:c.*13+976A>C	ENSP00000421671.1:n.*13+976A>C
ENST00000515059.6:c.*989A>C MANE Select	ENSP00000426617.1:n.*989A>C
ENST00000672698.1:c.*989A>C	ENSP00000500035.1:n.*989A>C
ENST00000440890.6:c.*989A>C	ENSP00000401907.2:n.*989A>C
ENST00000515059.5:c.*989A>C	ENSP00000426617.1:n.*989A>C
NM_001203.2:c.*989A>C	NP_001194.1:n.*989A>C
NM_001256792.1:c.*989A>C	NP_001243721.1:n.*989A>C
NM_001256793.1:c.*989A>C	NP_001243722.1:n.*989A>C
NM_001256794.1:c.*989A>C	NP_001243723.1:n.*989A>C
XM_011532201.1:c.*989A>C	XP_011530503.1:n.*989A>C
XM_011532202.1:c.*989A>C	XP_011530504.1:n.*989A>C
XM_011532201.2:c.*989A>C	XP_011530503.1:n.*989A>C
XM_017008558.1:c.*989A>C	XP_016864047.1:n.*989A>C
XM_017008559.1:c.*989A>C	XP_016864048.1:n.*989A>C
XM_017008560.1:c.*989A>C	XP_016864049.1:n.*989A>C
XM_017008561.1:c.*989A>C	XP_016864050.1:n.*989A>C
NM_001203.3:c.*989A>C MANE Select	NP_001194.1:n.*989A>C
NM_001256793.2:c.*989A>C	NP_001243722.1:n.*989A>C
NM_001256792.2:c.*989A>C	NP_001243721.1:n.*989A>C