Canonical Allele Identifier: CA2038861094
Gene: INHBC HGNC NCBI

Linked Data

dbSNP Id: rs1870684973
gnomAD v4: 12-57450274-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450274C>A , CM000674.2:g.57450274C>A GRCh38
NC_000012.11:g.57844057C>A , CM000674.1:g.57844057C>A GRCh37
NC_000012.10:g.56130324C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309668.3:c.*252C>A MANE Select ENSP00000308716.2:n.*252C>A
ENST00000309668.2:c.*252C>A ENSP00000308716.2:n.*252C>A
NM_005538.3:c.*252C>A NP_005529.1:n.*252C>A
NM_005538.4:c.*252C>A MANE Select NP_005529.1:n.*252C>A
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