Canonical Allele Identifier: CA3710222
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs183137172
gnomAD v2: 6-31236904-T-C
gnomAD v3: 6-31269127-T-C
gnomAD v4: 6-31269127-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269127T>C , CM000668.2:g.31269127T>C GRCh38
NC_000006.11:g.31236904T>C , CM000668.1:g.31236904T>C GRCh37
NC_000006.10:g.31344883T>C NCBI36
NG_029422.2:g.8005A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*42A>G MANE Select ENSP00000365402.5:n.*42A>G
ENST00000376228.9:c.*42A>G ENSP00000365402.5:n.*42A>G
ENST00000376237.8:c.*730A>G ENSP00000365412.4:n.*730A>G
ENST00000383329.7:c.*42A>G ENSP00000372819.3:n.*42A>G
ENST00000466892.5:n.376A>G
ENST00000470363.5:n.901A>G
ENST00000487245.5:n.1502A>G
NM_002117.5:c.*42A>G NP_002108.4:n.*42A>G
NM_002117.6:c.*42A>G MANE Select NP_002108.4:n.*42A>G