Canonical Allele Identifier: CA3710822
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs748848793
ExAC: 6:31239153 T / TC
gnomAD v2: 6-31239153-T-TC
gnomAD v3: 6-31271376-T-TC
gnomAD v4: 6-31271376-T-TC
COSMIC: COSN2535006
MyVariant Identifiers: chr6:g.31239153_31239154insC (hg19) chr6:g.31271376_31271377insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271381dup , CM000668.2:g.31271381dup GRCh38
NC_000006.11:g.31239158dup , CM000668.1:g.31239158dup GRCh37
NC_000006.10:g.31347137dup NCBI36
NG_029422.2:g.5755dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-29dup MANE Select ENSP00000365402.5:n.344-29dup
ENST00000376228.9:c.344-29dup ENSP00000365402.5:n.344-29dup
ENST00000376237.8:c.344-46dup ENSP00000365412.4:n.344-46dup
ENST00000383329.7:c.344-29dup ENSP00000372819.3:n.344-29dup
ENST00000415537.1:c.342-29dup
ENST00000484378.1:n.584dup
ENST00000487245.5:n.674dup
ENST00000495835.1:n.533-29dup
NM_002117.5:c.344-29dup NP_002108.4:n.344-29dup
NM_002117.6:c.344-29dup MANE Select NP_002108.4:n.344-29dup
Search 100 bp 5'
Search 100 bp 3'