Canonical Allele Identifier: CA2619452974
Gene: INHBC HGNC NCBI

Linked Data

gnomAD v4: 12-57450278-T-G
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000309668.3:c.*256T>G MANE Select ENSP00000308716.2:n.*256T>G
ENST00000309668.2:c.*256T>G ENSP00000308716.2:n.*256T>G
NM_005538.3:c.*256T>G NP_005529.1:n.*256T>G
NM_005538.4:c.*256T>G MANE Select NP_005529.1:n.*256T>G
Search 100 bp 5'
Search 100 bp 3'