Canonical Allele Identifier: CA1477875602
Gene: BMPR1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94935422T= , CM000666.2:g.94935422T= GRCh38
NC_000004.11:g.95856573T= , CM000666.1:g.95856573T= GRCh37
NC_000004.10:g.96075596T= NCBI36
NG_009245.1:g.182446T=

Transcript Alleles

HGVS Amino-acid change
ENST00000515059.6:c.-113+59522T= MANE Select ENSP00000426617.1:n.-113+59522T=
ENST00000515059.5:c.-113+59522T= ENSP00000426617.1:n.-113+59522T=
NM_001203.2:c.-113+59522T= NP_001194.1:n.-113+59522T=
XM_011532201.1:c.-18+59522T= XP_011530503.1:n.-18+59522T=
XM_011532201.2:c.-18+59522T= XP_011530503.1:n.-18+59522T=
XM_017008558.1:c.-113+59522T= XP_016864047.1:n.-113+59522T=
XM_017008559.1:c.-113+36372T= XP_016864048.1:n.-113+36372T=
NM_001203.3:c.-113+59522T= MANE Select NP_001194.1:n.-113+59522T=
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