Canonical Allele Identifier: CA2509455514
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935445_94935447del , CM000666.2:g.94935445_94935447del GRCh38
NC_000004.11:g.95856596_95856598del , CM000666.1:g.95856596_95856598del GRCh37
NC_000004.10:g.96075619_96075621del NCBI36
NG_009245.1:g.182469_182471del

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59545_-113+59547del MANE Select ENSP00000426617.1:n.-113+59545_-113+59547...
ENST00000515059.5:c.-113+59545_-113+59547del ENSP00000426617.1:n.-113+59545_-113+59547...
NM_001203.2:c.-113+59545_-113+59547del NP_001194.1:n.-113+59545_-113+59547del
XM_011532201.1:c.-18+59545_-18+59547del XP_011530503.1:n.-18+59545_-18+59547del
XM_011532201.2:c.-18+59545_-18+59547del XP_011530503.1:n.-18+59545_-18+59547del
XM_017008558.1:c.-113+59545_-113+59547del XP_016864047.1:n.-113+59545_-113+59547del...
XM_017008559.1:c.-113+36395_-113+36397del XP_016864048.1:n.-113+36395_-113+36397del...
NM_001203.3:c.-113+59545_-113+59547del MANE Select NP_001194.1:n.-113+59545_-113+59547del