Canonical Allele Identifier: CA3710382
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs12209550
ExAC: 6:31237824 C / T
gnomAD v2: 6-31237824-C-T
gnomAD v4: 6-31270047-C-T
MyVariant Identifiers: chr6:g.31237824C>T (hg19) chr6:g.31270047C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270047C>T , CM000668.2:g.31270047C>T GRCh38
NC_000006.11:g.31237824C>T , CM000668.1:g.31237824C>T GRCh37
NC_000006.10:g.31345803C>T NCBI36
NG_029422.2:g.7085G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.934G>A MANE Select ENSP00000365402.5:p.Val312Ile
ENST00000376228.9:c.934G>A ENSP00000365402.5:p.Val312Ile
ENST00000376237.8:c.*521G>A ENSP00000365412.4:n.*521G>A
ENST00000383329.7:c.934G>A ENSP00000372819.3:p.Val312Ile
ENST00000470363.5:n.252G>A
ENST00000487245.5:n.1293G>A
NM_002117.5:c.934G>A NP_002108.4:p.Val312Ile
NM_002117.6:c.934G>A MANE Select NP_002108.4:p.Val312Ile
Search 100 bp 5'
Search 100 bp 3'