Canonical Allele Identifier: CA1477857916
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935575_94935577delinsCAG , CM000666.2:g.94935575_94935577delinsCAG GRCh38
NC_000004.11:g.95856726_95856728delinsCAG , CM000666.1:g.95856726_95856728delinsCAG GRCh37
NC_000004.10:g.96075749_96075751delinsCAG NCBI36
NG_009245.1:g.182599_182601delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59675_-113+59677delinsCAG MANE Select ENSP00000426617.1:n.-113+59675_-113+59677...
ENST00000515059.5:c.-113+59675_-113+59677delinsCAG ENSP00000426617.1:n.-113+59675_-113+59677...
NM_001203.2:c.-113+59675_-113+59677delinsCAG NP_001194.1:n.-113+59675_-113+59677delins...
XM_011532201.1:c.-18+59675_-18+59677delinsCAG XP_011530503.1:n.-18+59675_-18+59677delin...
XM_011532201.2:c.-18+59675_-18+59677delinsCAG XP_011530503.1:n.-18+59675_-18+59677delin...
XM_017008558.1:c.-113+59675_-113+59677delinsCAG XP_016864047.1:n.-113+59675_-113+59677del...
XM_017008559.1:c.-113+36525_-113+36527delinsCAG XP_016864048.1:n.-113+36525_-113+36527del...
NM_001203.3:c.-113+59675_-113+59677delinsCAG MANE Select NP_001194.1:n.-113+59675_-113+59677delins...