Canonical Allele Identifier: CA823863486
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs767749366
gnomAD v4: 6-31271373-C-G
MyVariant Identifiers: chr6:g.31239150C>G (hg19) chr6:g.31271373C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271373C>G , CM000668.2:g.31271373C>G GRCh38
NC_000006.11:g.31239150C>G , CM000668.1:g.31239150C>G GRCh37
NC_000006.10:g.31347129C>G NCBI36
NG_029422.2:g.5759G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-25G>C MANE Select ENSP00000365402.5:n.344-25G>C
ENST00000376228.9:c.344-25G>C ENSP00000365402.5:n.344-25G>C
ENST00000376237.8:c.344-42G>C ENSP00000365412.4:n.344-42G>C
ENST00000383329.7:c.344-25G>C ENSP00000372819.3:n.344-25G>C
ENST00000415537.1:c.342-25G>C
ENST00000484378.1:n.588G>C
ENST00000487245.5:n.678G>C
ENST00000495835.1:n.533-25G>C
NM_002117.5:c.344-25G>C NP_002108.4:n.344-25G>C
NM_002117.6:c.344-25G>C MANE Select NP_002108.4:n.344-25G>C
Search 100 bp 5'
Search 100 bp 3'