Canonical Allele Identifier: CA3710234
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs765288380
ExAC: 6:31236959 C / CA
gnomAD v2: 6-31236959-C-CA
gnomAD v4: 6-31269182-C-CA
MyVariant Identifiers: chr6:g.31236959_31236960insA (hg19) chr6:g.31269182_31269183insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269183dup , CM000668.2:g.31269183dup GRCh38
NC_000006.11:g.31236960dup , CM000668.1:g.31236960dup GRCh37
NC_000006.10:g.31344939dup NCBI36
NG_029422.2:g.7949dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1097-10dup MANE Select ENSP00000365402.5:n.1097-10dup
ENST00000376228.9:c.1097-10dup ENSP00000365402.5:n.1097-10dup
ENST00000376237.8:c.*684-10dup ENSP00000365412.4:n.*684-10dup
ENST00000383329.7:c.1115-10dup ENSP00000372819.3:n.1115-10dup
ENST00000466892.5:n.330-10dup
ENST00000470363.5:n.855-10dup
ENST00000487245.5:n.1456-10dup
NM_002117.5:c.1097-10dup NP_002108.4:n.1097-10dup
NM_002117.6:c.1097-10dup MANE Select NP_002108.4:n.1097-10dup
Search 100 bp 5'
Search 100 bp 3'