Canonical Allele Identifier: CA1619077279
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761100035
gnomAD v4: 6-31269067-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269067C>T , CM000668.2:g.31269067C>T GRCh38
NC_000006.11:g.31236844C>T , CM000668.1:g.31236844C>T GRCh37
NC_000006.10:g.31344823C>T NCBI36
NG_029422.2:g.8065G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*102G>A MANE Select ENSP00000365402.5:n.*102G>A
ENST00000376228.9:c.*102G>A ENSP00000365402.5:n.*102G>A
ENST00000376237.8:c.*790G>A ENSP00000365412.4:n.*790G>A
ENST00000383329.7:c.*102G>A ENSP00000372819.3:n.*102G>A
ENST00000466892.5:n.436G>A
ENST00000470363.5:n.961G>A
ENST00000487245.5:n.1562G>A
NM_002117.5:c.*102G>A NP_002108.4:n.*102G>A
NM_002117.6:c.*102G>A MANE Select NP_002108.4:n.*102G>A
Search 100 bp 5'
Search 100 bp 3'