Canonical Allele Identifier: CA566336540
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1369042876
gnomAD v2: 6-31238438-T-C
gnomAD v3: 6-31270661-T-C
gnomAD v4: 6-31270661-T-C
MyVariant Identifiers: chr6:g.31238438T>C (hg19) chr6:g.31270661T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270661T>C , CM000668.2:g.31270661T>C GRCh38
NC_000006.11:g.31238438T>C , CM000668.1:g.31238438T>C GRCh37
NC_000006.10:g.31346417T>C NCBI36
NG_029422.2:g.6471A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-176A>G MANE Select ENSP00000365402.5:n.620-176A>G
ENST00000376228.9:c.620-176A>G ENSP00000365402.5:n.620-176A>G
ENST00000376237.8:c.*207-176A>G ENSP00000365412.4:n.*207-176A>G
ENST00000383329.7:c.620-176A>G ENSP00000372819.3:n.620-176A>G
ENST00000415537.1:c.618-176A>G
ENST00000487245.5:n.979-176A>G
ENST00000495835.1:n.809-176A>G
NM_002117.5:c.620-176A>G NP_002108.4:n.620-176A>G
NM_002117.6:c.620-176A>G MANE Select NP_002108.4:n.620-176A>G
Search 100 bp 5'
Search 100 bp 3'