Canonical Allele Identifier: CA449609561
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269363-A-C
MyVariant Identifiers: chr6:g.31237140A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269363A>C , CM000668.2:g.31269363A>C GRCh38
NC_000006.11:g.31237140A>C , CM000668.1:g.31237140A>C GRCh37
NC_000006.10:g.31345119A>C NCBI36
NG_029422.2:g.7769T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1071T>G MANE Select ENSP00000365402.5:p.Ser357=
ENST00000376228.9:c.1071T>G ENSP00000365402.5:p.Ser357=
ENST00000376237.8:c.*658T>G ENSP00000365412.4:n.*658T>G
ENST00000383329.7:c.1089T>G ENSP00000372819.3:p.Ser363=
ENST00000466892.5:n.304T>G
ENST00000470363.5:n.829T>G
ENST00000487245.5:n.1430T>G
NM_002117.5:c.1071T>G NP_002108.4:p.Ser357=
NM_002117.6:c.1071T>G MANE Select NP_002108.4:p.Ser357=
Search 100 bp 5'
Search 100 bp 3'