Canonical Allele Identifier: CA3710436
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9264626
ExAC: 6:31237962 T / C
gnomAD v2: 6-31237962-T-C
gnomAD v3: 6-31270185-T-C
gnomAD v4: 6-31270185-T-C
MyVariant Identifiers: chr6:g.31237962T>C (hg19) chr6:g.31237962_31237966delinsCGTGA (hg19) chr6:g.31270185T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270185T>C , CM000668.2:g.31270185T>C GRCh38
NC_000006.11:g.31237962T>C , CM000668.1:g.31237962T>C GRCh37
NC_000006.10:g.31345941T>C NCBI36
NG_029422.2:g.6947A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+25A>G MANE Select ENSP00000365402.5:n.895+25A>G
ENST00000376228.9:c.895+25A>G ENSP00000365402.5:n.895+25A>G
ENST00000376237.8:c.*482+25A>G ENSP00000365412.4:n.*482+25A>G
ENST00000383329.7:c.895+25A>G ENSP00000372819.3:n.895+25A>G
ENST00000470363.5:n.213+25A>G
ENST00000487245.5:n.1254+25A>G
NM_002117.5:c.895+25A>G NP_002108.4:n.895+25A>G
NM_002117.6:c.895+25A>G MANE Select NP_002108.4:n.895+25A>G
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