Canonical Allele Identifier: CA1619080597
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761341839
gnomAD v4: 6-31271397-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271397C>A , CM000668.2:g.31271397C>A GRCh38
NC_000006.11:g.31239174C>A , CM000668.1:g.31239174C>A GRCh37
NC_000006.10:g.31347153C>A NCBI36
NG_029422.2:g.5735G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-49G>T MANE Select ENSP00000365402.5:n.344-49G>T
ENST00000376228.9:c.344-49G>T ENSP00000365402.5:n.344-49G>T
ENST00000376237.8:c.344-66G>T ENSP00000365412.4:n.344-66G>T
ENST00000383329.7:c.344-49G>T ENSP00000372819.3:n.344-49G>T
ENST00000415537.1:c.342-49G>T
ENST00000484378.1:n.564G>T
ENST00000487245.5:n.654G>T
ENST00000495835.1:n.533-49G>T
NM_002117.5:c.344-49G>T NP_002108.4:n.344-49G>T
NM_002117.6:c.344-49G>T MANE Select NP_002108.4:n.344-49G>T