Canonical Allele Identifier: CA823863614
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1410976458
gnomAD v3: 6-31271449-G-T
gnomAD v4: 6-31271449-G-T
MyVariant Identifiers: chr6:g.31239226G>T (hg19) chr6:g.31271449G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271449G>T , CM000668.2:g.31271449G>T GRCh38
NC_000006.11:g.31239226G>T , CM000668.1:g.31239226G>T GRCh37
NC_000006.10:g.31347205G>T NCBI36
NG_029422.2:g.5683C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-101C>A MANE Select ENSP00000365402.5:n.344-101C>A
ENST00000376228.9:c.344-101C>A ENSP00000365402.5:n.344-101C>A
ENST00000376237.8:c.344-118C>A ENSP00000365412.4:n.344-118C>A
ENST00000383329.7:c.344-101C>A ENSP00000372819.3:n.344-101C>A
ENST00000415537.1:c.342-101C>A
ENST00000484378.1:n.512C>A
ENST00000487245.5:n.602C>A
ENST00000495835.1:n.533-101C>A
NM_002117.5:c.344-101C>A NP_002108.4:n.344-101C>A
NM_002117.6:c.344-101C>A MANE Select NP_002108.4:n.344-101C>A
Search 100 bp 5'
Search 100 bp 3'