Canonical Allele Identifier: CA1477875586
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935388C= , CM000666.2:g.94935388C= GRCh38
NC_000004.11:g.95856539C= , CM000666.1:g.95856539C= GRCh37
NC_000004.10:g.96075562C= NCBI36
NG_009245.1:g.182412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515059.6:c.-113+59488C= MANE Select ENSP00000426617.1:n.-113+59488C=
ENST00000515059.5:c.-113+59488C= ENSP00000426617.1:n.-113+59488C=
NM_001203.2:c.-113+59488C= NP_001194.1:n.-113+59488C=
XM_011532201.1:c.-18+59488C= XP_011530503.1:n.-18+59488C=
XM_011532201.2:c.-18+59488C= XP_011530503.1:n.-18+59488C=
XM_017008558.1:c.-113+59488C= XP_016864047.1:n.-113+59488C=
XM_017008559.1:c.-113+36338C= XP_016864048.1:n.-113+36338C=
NM_001203.3:c.-113+59488C= MANE Select NP_001194.1:n.-113+59488C=