Canonical Allele Identifier: CA2677951486
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2113912460
gnomAD v4: 6-31271444-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271444T>A , CM000668.2:g.31271444T>A GRCh38
NC_000006.11:g.31239221T>A , CM000668.1:g.31239221T>A GRCh37
NC_000006.10:g.31347200T>A NCBI36
NG_029422.2:g.5688A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-96A>T MANE Select ENSP00000365402.5:n.344-96A>T
ENST00000376228.9:c.344-96A>T ENSP00000365402.5:n.344-96A>T
ENST00000376237.8:c.344-113A>T ENSP00000365412.4:n.344-113A>T
ENST00000383329.7:c.344-96A>T ENSP00000372819.3:n.344-96A>T
ENST00000415537.1:c.342-96A>T
ENST00000484378.1:n.517A>T
ENST00000487245.5:n.607A>T
ENST00000495835.1:n.533-96A>T
NM_002117.5:c.344-96A>T NP_002108.4:n.344-96A>T
NM_002117.6:c.344-96A>T MANE Select NP_002108.4:n.344-96A>T