Canonical Allele Identifier: CA449609791
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269521-T-G
gnomAD v4: 6-31269521-T-G
MyVariant Identifiers: chr6:g.31237298T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269521T>G , CM000668.2:g.31269521T>G GRCh38
NC_000006.11:g.31237298T>G , CM000668.1:g.31237298T>G GRCh37
NC_000006.10:g.31345277T>G NCBI36
NG_029422.2:g.7611A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1020A>C MANE Select ENSP00000365402.5:p.Gly340=
ENST00000376228.9:c.1020A>C ENSP00000365402.5:p.Gly340=
ENST00000376237.8:c.*607A>C ENSP00000365412.4:n.*607A>C
ENST00000383329.7:c.1038A>C ENSP00000372819.3:p.Gly346=
ENST00000466892.5:n.146A>C
ENST00000470363.5:n.778A>C
ENST00000487245.5:n.1379A>C
NM_002117.5:c.1020A>C NP_002108.4:p.Gly340=
NM_002117.6:c.1020A>C MANE Select NP_002108.4:p.Gly340=
Search 100 bp 5'
Search 100 bp 3'