Canonical Allele Identifier: CA363322728
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270456-G-C
MyVariant Identifiers: chr6:g.31238233G>C (hg19) chr6:g.31270456G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270456G>C , CM000668.2:g.31270456G>C GRCh38
NC_000006.11:g.31238233G>C , CM000668.1:g.31238233G>C GRCh37
NC_000006.10:g.31346212G>C NCBI36
NG_029422.2:g.6676C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.649C>G MANE Select ENSP00000365402.5:p.Pro217Ala
ENST00000376228.9:c.649C>G ENSP00000365402.5:p.Pro217Ala
ENST00000376237.8:c.*236C>G ENSP00000365412.4:n.*236C>G
ENST00000383329.7:c.649C>G ENSP00000372819.3:p.Pro217Ala
ENST00000415537.1:c.647C>G
ENST00000487245.5:n.1008C>G
ENST00000495835.1:n.838C>G
NM_002117.5:c.649C>G NP_002108.4:p.Pro217Ala
NM_002117.6:c.649C>G MANE Select NP_002108.4:p.Pro217Ala
Search 100 bp 5'
Search 100 bp 3'