Canonical Allele Identifier: CA566688958
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1326761719
gnomAD v2: 6-31237890-C-G
gnomAD v4: 6-31270113-C-G
MyVariant Identifiers: chr6:g.31237890C>G (hg19) chr6:g.31270113C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270113C>G , CM000668.2:g.31270113C>G GRCh38
NC_000006.11:g.31237890C>G , CM000668.1:g.31237890C>G GRCh37
NC_000006.10:g.31345869C>G NCBI36
NG_029422.2:g.7019G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896-28G>C MANE Select ENSP00000365402.5:n.896-28G>C
ENST00000376228.9:c.896-28G>C ENSP00000365402.5:n.896-28G>C
ENST00000376237.8:c.*483-28G>C ENSP00000365412.4:n.*483-28G>C
ENST00000383329.7:c.896-28G>C ENSP00000372819.3:n.896-28G>C
ENST00000470363.5:n.214-28G>C
ENST00000487245.5:n.1255-28G>C
NM_002117.5:c.896-28G>C NP_002108.4:n.896-28G>C
NM_002117.6:c.896-28G>C MANE Select NP_002108.4:n.896-28G>C
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