Canonical Allele Identifier: CA2619452966
Gene: INHBC HGNC NCBI

Linked Data

gnomAD v4: 12-57450275-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450275C>G , CM000674.2:g.57450275C>G GRCh38
NC_000012.11:g.57844058C>G , CM000674.1:g.57844058C>G GRCh37
NC_000012.10:g.56130325C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309668.3:c.*253C>G MANE Select ENSP00000308716.2:n.*253C>G
ENST00000309668.2:c.*253C>G ENSP00000308716.2:n.*253C>G
NM_005538.3:c.*253C>G NP_005529.1:n.*253C>G
NM_005538.4:c.*253C>G MANE Select NP_005529.1:n.*253C>G
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