Canonical Allele Identifier: CA15437646
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1130580
gnomAD v2: 6-31236679-T-C
gnomAD v3: 6-31268902-T-C
gnomAD v4: 6-31268902-T-C
MyVariant Identifiers: chr6:g.31236679T>C (hg19) chr6:g.31268902T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268902T>C , CM000668.2:g.31268902T>C GRCh38
NC_000006.11:g.31236679T>C , CM000668.1:g.31236679T>C GRCh37
NC_000006.10:g.31344658T>C NCBI36
NG_029422.2:g.8230A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*267A>G MANE Select ENSP00000365402.5:n.*267A>G
ENST00000376228.9:c.*267A>G ENSP00000365402.5:n.*267A>G
ENST00000376237.8:c.*955A>G ENSP00000365412.4:n.*955A>G
ENST00000383329.7:c.*267A>G ENSP00000372819.3:n.*267A>G
ENST00000466892.5:n.601A>G
ENST00000470363.5:n.1126A>G
ENST00000487245.5:n.1727A>G
NM_002117.5:c.*267A>G NP_002108.4:n.*267A>G
NM_002117.6:c.*267A>G MANE Select NP_002108.4:n.*267A>G
Search 100 bp 5'
Search 100 bp 3'