Canonical Allele Identifier: CA449790325
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271158-C-T
gnomAD v4: 6-31271158-C-T
MyVariant Identifiers: chr6:g.31238935C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271158C>T , CM000668.2:g.31271158C>T GRCh38
NC_000006.11:g.31238935C>T , CM000668.1:g.31238935C>T GRCh37
NC_000006.10:g.31346914C>T NCBI36
NG_029422.2:g.5974G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.534G>A MANE Select ENSP00000365402.5:p.Glu178=
ENST00000376228.9:c.534G>A ENSP00000365402.5:p.Glu178=
ENST00000376237.8:c.*121G>A ENSP00000365412.4:n.*121G>A
ENST00000383329.7:c.534G>A ENSP00000372819.3:p.Glu178=
ENST00000415537.1:c.532G>A
ENST00000484378.1:n.803G>A
ENST00000487245.5:n.893G>A
ENST00000495835.1:n.723G>A
NM_002117.5:c.534G>A NP_002108.4:p.Glu178=
NM_002117.6:c.534G>A MANE Select NP_002108.4:p.Glu178=
Search 100 bp 5'
Search 100 bp 3'