Canonical Allele Identifier: CA566689032
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs200646093
gnomAD v2: 6-31239133-C-G
gnomAD v3: 6-31271356-C-G
gnomAD v4: 6-31271356-C-G
MyVariant Identifiers: chr6:g.31239133C>G (hg19) chr6:g.31271356C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271356C>G , CM000668.2:g.31271356C>G GRCh38
NC_000006.11:g.31239133C>G , CM000668.1:g.31239133C>G GRCh37
NC_000006.10:g.31347112C>G NCBI36
NG_029422.2:g.5776G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-8G>C MANE Select ENSP00000365402.5:n.344-8G>C
ENST00000376228.9:c.344-8G>C ENSP00000365402.5:n.344-8G>C
ENST00000376237.8:c.344-25G>C ENSP00000365412.4:n.344-25G>C
ENST00000383329.7:c.344-8G>C ENSP00000372819.3:n.344-8G>C
ENST00000415537.1:c.342-8G>C
ENST00000484378.1:n.605G>C
ENST00000487245.5:n.695G>C
ENST00000495835.1:n.533-8G>C
NM_002117.5:c.344-8G>C NP_002108.4:n.344-8G>C
NM_002117.6:c.344-8G>C MANE Select NP_002108.4:n.344-8G>C
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