Canonical Allele Identifier: CA1477875590
Gene: BMPR1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935393A= , CM000666.2:g.94935393A= GRCh38
NC_000004.11:g.95856544A= , CM000666.1:g.95856544A= GRCh37
NC_000004.10:g.96075567A= NCBI36
NG_009245.1:g.182417A=

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59493A= MANE Select ENSP00000426617.1:n.-113+59493A=
ENST00000515059.5:c.-113+59493A= ENSP00000426617.1:n.-113+59493A=
NM_001203.2:c.-113+59493A= NP_001194.1:n.-113+59493A=
XM_011532201.1:c.-18+59493A= XP_011530503.1:n.-18+59493A=
XM_011532201.2:c.-18+59493A= XP_011530503.1:n.-18+59493A=
XM_017008558.1:c.-113+59493A= XP_016864047.1:n.-113+59493A=
XM_017008559.1:c.-113+36343A= XP_016864048.1:n.-113+36343A=
NM_001203.3:c.-113+59493A= MANE Select NP_001194.1:n.-113+59493A=
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