Canonical Allele Identifier: CA3710808
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9264661
ExAC: 6:31239141 C / T
gnomAD v2: 6-31239141-C-T
gnomAD v3: 6-31271364-C-T
gnomAD v4: 6-31271364-C-T
MyVariant Identifiers: chr6:g.31239141C>T (hg19) chr6:g.31271364C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271364C>T , CM000668.2:g.31271364C>T GRCh38
NC_000006.11:g.31239141C>T , CM000668.1:g.31239141C>T GRCh37
NC_000006.10:g.31347120C>T NCBI36
NG_029422.2:g.5768G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-16G>A MANE Select ENSP00000365402.5:n.344-16G>A
ENST00000376228.9:c.344-16G>A ENSP00000365402.5:n.344-16G>A
ENST00000376237.8:c.344-33G>A ENSP00000365412.4:n.344-33G>A
ENST00000383329.7:c.344-16G>A ENSP00000372819.3:n.344-16G>A
ENST00000415537.1:c.342-16G>A
ENST00000484378.1:n.597G>A
ENST00000487245.5:n.687G>A
ENST00000495835.1:n.533-16G>A
NM_002117.5:c.344-16G>A NP_002108.4:n.344-16G>A
NM_002117.6:c.344-16G>A MANE Select NP_002108.4:n.344-16G>A
Search 100 bp 5'
Search 100 bp 3'