Canonical Allele Identifier: CA3710599
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs770450067
ExAC: 6:31238265 GA / G
gnomAD v2: 6-31238265-GA-G
gnomAD v4: 6-31270488-GA-G
MyVariant Identifiers: chr6:g.31238266del (hg19) chr6:g.31270489del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270489del , CM000668.2:g.31270489del GRCh38
NC_000006.11:g.31238266del , CM000668.1:g.31238266del GRCh37
NC_000006.10:g.31346245del NCBI36
NG_029422.2:g.6643del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.620-4del MANE Select ENSP00000365402.5:n.620-4del
ENST00000376228.9:c.620-4del ENSP00000365402.5:n.620-4del
ENST00000376237.8:c.*207-4del ENSP00000365412.4:n.*207-4del
ENST00000383329.7:c.620-4del ENSP00000372819.3:n.620-4del
ENST00000415537.1:c.618-4del
ENST00000487245.5:n.979-4del
ENST00000495835.1:n.809-4del
NM_002117.5:c.620-4del NP_002108.4:n.620-4del
NM_002117.6:c.620-4del MANE Select NP_002108.4:n.620-4del
Search 100 bp 5'
Search 100 bp 3'