Canonical Allele Identifier: CA823863527
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs745707117
gnomAD v4: 6-31271388-C-G
MyVariant Identifiers: chr6:g.31239165C>G (hg19) chr6:g.31271388C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271388C>G , CM000668.2:g.31271388C>G GRCh38
NC_000006.11:g.31239165C>G , CM000668.1:g.31239165C>G GRCh37
NC_000006.10:g.31347144C>G NCBI36
NG_029422.2:g.5744G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-40G>C MANE Select ENSP00000365402.5:n.344-40G>C
ENST00000376228.9:c.344-40G>C ENSP00000365402.5:n.344-40G>C
ENST00000376237.8:c.344-57G>C ENSP00000365412.4:n.344-57G>C
ENST00000383329.7:c.344-40G>C ENSP00000372819.3:n.344-40G>C
ENST00000415537.1:c.342-40G>C
ENST00000484378.1:n.573G>C
ENST00000487245.5:n.663G>C
ENST00000495835.1:n.533-40G>C
NM_002117.5:c.344-40G>C NP_002108.4:n.344-40G>C
NM_002117.6:c.344-40G>C MANE Select NP_002108.4:n.344-40G>C
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