Canonical Allele Identifier: CA2619452967
Gene: INHBC HGNC NCBI

Linked Data

gnomAD v4: 12-57450276-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450276A>C , CM000674.2:g.57450276A>C GRCh38
NC_000012.11:g.57844059A>C , CM000674.1:g.57844059A>C GRCh37
NC_000012.10:g.56130326A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309668.3:c.*254A>C MANE Select ENSP00000308716.2:n.*254A>C
ENST00000309668.2:c.*254A>C ENSP00000308716.2:n.*254A>C
NM_005538.3:c.*254A>C NP_005529.1:n.*254A>C
NM_005538.4:c.*254A>C MANE Select NP_005529.1:n.*254A>C
Search 100 bp 5'
Search 100 bp 3'