Canonical Allele Identifier: CA1477857871
Gene: BMPR1B HGNC NCBI

Linked Data

dbSNP Id: rs1729260032

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935524_94935525del , CM000666.2:g.94935524_94935525del GRCh38
NC_000004.11:g.95856675_95856676del , CM000666.1:g.95856675_95856676del GRCh37
NC_000004.10:g.96075698_96075699del NCBI36
NG_009245.1:g.182548_182549del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515059.6:c.-113+59624_-113+59625del MANE Select ENSP00000426617.1:n.-113+59624_-113+59625del
ENST00000515059.5:c.-113+59624_-113+59625del ENSP00000426617.1:n.-113+59624_-113+59625del
NM_001203.2:c.-113+59624_-113+59625del NP_001194.1:n.-113+59624_-113+59625del
XM_011532201.1:c.-18+59624_-18+59625del XP_011530503.1:n.-18+59624_-18+59625del
XM_011532201.2:c.-18+59624_-18+59625del XP_011530503.1:n.-18+59624_-18+59625del
XM_017008558.1:c.-113+59624_-113+59625del XP_016864047.1:n.-113+59624_-113+59625del
XM_017008559.1:c.-113+36474_-113+36475del XP_016864048.1:n.-113+36474_-113+36475del
NM_001203.3:c.-113+59624_-113+59625del MANE Select NP_001194.1:n.-113+59624_-113+59625del