Canonical Allele Identifier: CA3710252
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41548117
ExAC: 6:31237100 TC / T
gnomAD v2: 6-31237100-TC-T
gnomAD v3: 6-31269323-TC-T
gnomAD v4: 6-31269323-TC-T
MyVariant Identifiers: chr6:g.31237101del (hg19) chr6:g.31269325del (hg38) chr6:g.31269324del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269327del , CM000668.2:g.31269327del GRCh38
NC_000006.11:g.31237104del , CM000668.1:g.31237104del GRCh37
NC_000006.10:g.31345083del NCBI36
NG_029422.2:g.7808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+14del MANE Select ENSP00000365402.5:n.1096+14del
ENST00000376228.9:c.1096+14del ENSP00000365402.5:n.1096+14del
ENST00000376237.8:c.*683+14del ENSP00000365412.4:n.*683+14del
ENST00000383329.7:c.1114+14del ENSP00000372819.3:n.1114+14del
ENST00000466892.5:n.329+14del
ENST00000470363.5:n.854+14del
ENST00000487245.5:n.1455+14del
NM_002117.5:c.1096+14del NP_002108.4:n.1096+14del
NM_002117.6:c.1096+14del MANE Select NP_002108.4:n.1096+14del
Search 100 bp 5'
Search 100 bp 3'