Canonical Allele Identifier: CA2619452977
Gene: INHBC HGNC NCBI

Linked Data

gnomAD v4: 12-57450279-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450279C>T , CM000674.2:g.57450279C>T GRCh38
NC_000012.11:g.57844062C>T , CM000674.1:g.57844062C>T GRCh37
NC_000012.10:g.56130329C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309668.3:c.*257C>T MANE Select ENSP00000308716.2:n.*257C>T
ENST00000309668.2:c.*257C>T ENSP00000308716.2:n.*257C>T
NM_005538.3:c.*257C>T NP_005529.1:n.*257C>T
NM_005538.4:c.*257C>T MANE Select NP_005529.1:n.*257C>T
Search 100 bp 5'
Search 100 bp 3'