Canonical Allele Identifier: CA1477857908
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935562_94935563delinsCA , CM000666.2:g.94935562_94935563delinsCA GRCh38
NC_000004.11:g.95856713_95856714delinsCA , CM000666.1:g.95856713_95856714delinsCA GRCh37
NC_000004.10:g.96075736_96075737delinsCA NCBI36
NG_009245.1:g.182586_182587delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59662_-113+59663delinsCA MANE Select ENSP00000426617.1:n.-113+59662_-113+59663...
ENST00000515059.5:c.-113+59662_-113+59663delinsCA ENSP00000426617.1:n.-113+59662_-113+59663...
NM_001203.2:c.-113+59662_-113+59663delinsCA NP_001194.1:n.-113+59662_-113+59663delins...
XM_011532201.1:c.-18+59662_-18+59663delinsCA XP_011530503.1:n.-18+59662_-18+59663delin...
XM_011532201.2:c.-18+59662_-18+59663delinsCA XP_011530503.1:n.-18+59662_-18+59663delin...
XM_017008558.1:c.-113+59662_-113+59663delinsCA XP_016864047.1:n.-113+59662_-113+59663del...
XM_017008559.1:c.-113+36512_-113+36513delinsCA XP_016864048.1:n.-113+36512_-113+36513del...
NM_001203.3:c.-113+59662_-113+59663delinsCA MANE Select NP_001194.1:n.-113+59662_-113+59663delins...