Canonical Allele Identifier: CA3710827
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs768414447
ExAC: 6:31239160 A / AGCCCC
gnomAD v2: 6-31239160-A-AGCCCC
gnomAD v3: 6-31271383-A-AGCCCC
gnomAD v4: 6-31271383-A-AGCCCC
MyVariant Identifiers: chr6:g.31239165_31239166insGCCCC (hg19) chr6:g.31239160_31239161insGCCCC (hg19) chr6:g.31271388_31271389insGCCCC (hg38) chr6:g.31271383_31271384insGCCCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271395_31271399dup , CM000668.2:g.31271395_31271399dup GRCh38
NC_000006.11:g.31239172_31239176dup , CM000668.1:g.31239172_31239176dup GRCh37
NC_000006.10:g.31347151_31347155dup NCBI36
NG_029422.2:g.5744_5748dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-40_344-36dup MANE Select ENSP00000365402.5:n.344-40_344-36dup
ENST00000376228.9:c.344-40_344-36dup ENSP00000365402.5:n.344-40_344-36dup
ENST00000376237.8:c.344-57_344-53dup ENSP00000365412.4:n.344-57_344-53dup
ENST00000383329.7:c.344-40_344-36dup ENSP00000372819.3:n.344-40_344-36dup
ENST00000415537.1:c.342-40_342-36dup
ENST00000484378.1:n.573_577dup
ENST00000487245.5:n.663_667dup
ENST00000495835.1:n.533-40_533-36dup
NM_002117.5:c.344-40_344-36dup NP_002108.4:n.344-40_344-36dup
NM_002117.6:c.344-40_344-36dup MANE Select NP_002108.4:n.344-40_344-36dup
Search 100 bp 5'
Search 100 bp 3'