Canonical Allele Identifier: CA823863590
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1339870865
gnomAD v3: 6-31271414-A-AT
gnomAD v4: 6-31271414-A-AT
MyVariant Identifiers: chr6:g.31239191_31239192insT (hg19) chr6:g.31271414_31271415insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271418dup , CM000668.2:g.31271418dup GRCh38
NC_000006.11:g.31239195dup , CM000668.1:g.31239195dup GRCh37
NC_000006.10:g.31347174dup NCBI36
NG_029422.2:g.5717dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-67dup MANE Select ENSP00000365402.5:n.344-67dup
ENST00000376228.9:c.344-67dup ENSP00000365402.5:n.344-67dup
ENST00000376237.8:c.344-84dup ENSP00000365412.4:n.344-84dup
ENST00000383329.7:c.344-67dup ENSP00000372819.3:n.344-67dup
ENST00000415537.1:c.342-67dup
ENST00000484378.1:n.546dup
ENST00000487245.5:n.636dup
ENST00000495835.1:n.533-67dup
NM_002117.5:c.344-67dup NP_002108.4:n.344-67dup
NM_002117.6:c.344-67dup MANE Select NP_002108.4:n.344-67dup
Search 100 bp 5'
Search 100 bp 3'