Canonical Allele Identifier: CA2677949082
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2113900207
gnomAD v4: 6-31268898-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268898T>A , CM000668.2:g.31268898T>A GRCh38
NC_000006.11:g.31236675T>A , CM000668.1:g.31236675T>A GRCh37
NC_000006.10:g.31344654T>A NCBI36
NG_029422.2:g.8234A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*271A>T MANE Select ENSP00000365402.5:n.*271A>T
ENST00000376228.9:c.*271A>T ENSP00000365402.5:n.*271A>T
ENST00000376237.8:c.*959A>T ENSP00000365412.4:n.*959A>T
ENST00000383329.7:c.*271A>T ENSP00000372819.3:n.*271A>T
ENST00000466892.5:n.605A>T
ENST00000470363.5:n.1130A>T
ENST00000487245.5:n.1731A>T
NM_002117.5:c.*271A>T NP_002108.4:n.*271A>T
NM_002117.6:c.*271A>T MANE Select NP_002108.4:n.*271A>T
Search 100 bp 5'
Search 100 bp 3'