Canonical Allele Identifier: CA449790248
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270238-C-G
MyVariant Identifiers: chr6:g.31238015C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270238C>G , CM000668.2:g.31270238C>G GRCh38
NC_000006.11:g.31238015C>G , CM000668.1:g.31238015C>G GRCh37
NC_000006.10:g.31345994C>G NCBI36
NG_029422.2:g.6894G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.867G>C MANE Select ENSP00000365402.5:p.Gly289=
ENST00000376228.9:c.867G>C ENSP00000365402.5:p.Gly289=
ENST00000376237.8:c.*454G>C ENSP00000365412.4:n.*454G>C
ENST00000383329.7:c.867G>C ENSP00000372819.3:p.Gly289=
ENST00000415537.1:c.758G>C
ENST00000470363.5:n.185G>C
ENST00000487245.5:n.1226G>C
ENST00000495835.1:n.1056G>C
NM_002117.5:c.867G>C NP_002108.4:p.Gly289=
NM_002117.6:c.867G>C MANE Select NP_002108.4:p.Gly289=
Search 100 bp 5'
Search 100 bp 3'