Canonical Allele Identifier: CA2619452973

Gene: INHBC

Linked Data

• gnomAD v4: 12-57450278-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57450278T>C , CM000674.2:g.57450278T>C	GRCh38
NC_000012.11:g.57844061T>C , CM000674.1:g.57844061T>C	GRCh37
NC_000012.10:g.56130328T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309668.3:c.*256T>C MANE Select	ENSP00000308716.2:n.*256T>C
ENST00000309668.2:c.*256T>C	ENSP00000308716.2:n.*256T>C
NM_005538.3:c.*256T>C	NP_005529.1:n.*256T>C
NM_005538.4:c.*256T>C MANE Select	NP_005529.1:n.*256T>C