Canonical Allele Identifier: CA136866504
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860527
gnomAD v2: 6-31238905-G-T
gnomAD v3: 6-31271128-G-T
gnomAD v4: 6-31271128-G-T
MyVariant Identifiers: chr6:g.31238905G>T (hg19) chr6:g.31271128G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271128G>T , CM000668.2:g.31271128G>T GRCh38
NC_000006.11:g.31238905G>T , CM000668.1:g.31238905G>T GRCh37
NC_000006.10:g.31346884G>T NCBI36
NG_029422.2:g.6004C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.564C>A MANE Select ENSP00000365402.5:p.Cys188Ter
ENST00000376228.9:c.564C>A ENSP00000365402.5:p.Cys188Ter
ENST00000376237.8:c.*151C>A ENSP00000365412.4:n.*151C>A
ENST00000383329.7:c.564C>A ENSP00000372819.3:p.Cys188Ter
ENST00000415537.1:c.562C>A
ENST00000484378.1:n.833C>A
ENST00000487245.5:n.923C>A
ENST00000495835.1:n.753C>A
NM_002117.5:c.564C>A NP_002108.4:p.Cys188Ter
NM_002117.6:c.564C>A MANE Select NP_002108.4:p.Cys188Ter
Search 100 bp 5'
Search 100 bp 3'