Canonical Allele Identifier: CA3014920
Gene: BMPR1B HGNC NCBI

Linked Data

ClinVar Variation Id: 283921
dbSNP Id: rs570808649
gnomAD v2: 4-96036832-A-G
gnomAD v3: 4-95115681-A-G
gnomAD v4: 4-95115681-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95115681A>G , CM000666.2:g.95115681A>G GRCh38
NC_000004.11:g.96036832A>G , CM000666.1:g.96036832A>G GRCh37
NC_000004.10:g.96255855A>G NCBI36
NG_009245.1:g.362705A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000440890.7:c.337-4A>G ENSP00000401907.2:n.337-4A>G
ENST00000502683.6:n.463-4A>G
ENST00000509540.6:c.247-4A>G ENSP00000421671.1:n.247-4A>G
ENST00000515059.6:c.247-4A>G MANE Select ENSP00000426617.1:n.247-4A>G
ENST00000672698.1:c.247-4A>G ENSP00000500035.1:n.247-4A>G
ENST00000264568.8:c.247-4A>G ENSP00000264568.4:n.247-4A>G
ENST00000394931.1:c.247-4A>G ENSP00000378389.1:n.247-4A>G
ENST00000440890.6:c.337-4A>G ENSP00000401907.2:n.337-4A>G
ENST00000502683.5:c.252-4A>G ENSP00000424693.1:n.252-4A>G
ENST00000506363.5:c.247-4A>G ENSP00000421144.1:n.247-4A>G
ENST00000509540.5:c.247-4A>G ENSP00000421671.1:n.247-4A>G
ENST00000512312.5:c.247-4A>G ENSP00000425444.1:n.247-4A>G
ENST00000515059.5:c.247-4A>G ENSP00000426617.1:n.247-4A>G
NM_001203.2:c.247-4A>G NP_001194.1:n.247-4A>G
NM_001256792.1:c.247-4A>G NP_001243721.1:n.247-4A>G
NM_001256793.1:c.337-4A>G NP_001243722.1:n.337-4A>G
NM_001256794.1:c.247-4A>G NP_001243723.1:n.247-4A>G
XM_011532201.1:c.247-4A>G XP_011530503.1:n.247-4A>G
XM_011532202.1:c.247-4A>G XP_011530504.1:n.247-4A>G
XM_011532201.2:c.247-4A>G XP_011530503.1:n.247-4A>G
XM_017008558.1:c.247-4A>G XP_016864047.1:n.247-4A>G
XM_017008559.1:c.247-4A>G XP_016864048.1:n.247-4A>G
XM_017008560.1:c.247-4A>G XP_016864049.1:n.247-4A>G
XM_017008561.1:c.247-4A>G XP_016864050.1:n.247-4A>G
NM_001203.3:c.247-4A>G MANE Select NP_001194.1:n.247-4A>G
NM_001256793.2:c.337-4A>G NP_001243722.1:n.337-4A>G
NM_001256792.2:c.247-4A>G NP_001243721.1:n.247-4A>G