Canonical Allele Identifier: CA449609593
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269372-G-T
MyVariant Identifiers: chr6:g.31237149G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269372G>T , CM000668.2:g.31269372G>T GRCh38
NC_000006.11:g.31237149G>T , CM000668.1:g.31237149G>T GRCh37
NC_000006.10:g.31345128G>T NCBI36
NG_029422.2:g.7760C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1062C>A MANE Select ENSP00000365402.5:p.Ala354=
ENST00000376228.9:c.1062C>A ENSP00000365402.5:p.Ala354=
ENST00000376237.8:c.*649C>A ENSP00000365412.4:n.*649C>A
ENST00000383329.7:c.1080C>A ENSP00000372819.3:p.Ala360=
ENST00000466892.5:n.295C>A
ENST00000470363.5:n.820C>A
ENST00000487245.5:n.1421C>A
NM_002117.5:c.1062C>A NP_002108.4:p.Ala354=
NM_002117.6:c.1062C>A MANE Select NP_002108.4:p.Ala354=
Search 100 bp 5'
Search 100 bp 3'