Canonical Allele Identifier: CA363319863
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs45485294
gnomAD v2: 6-31237848-G-T
gnomAD v3: 6-31270071-G-T
gnomAD v4: 6-31270071-G-T
MyVariant Identifiers: chr6:g.31237848G>T (hg19) chr6:g.31270071G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270071G>T , CM000668.2:g.31270071G>T GRCh38
NC_000006.11:g.31237848G>T , CM000668.1:g.31237848G>T GRCh37
NC_000006.10:g.31345827G>T NCBI36
NG_029422.2:g.7061C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.910C>A MANE Select ENSP00000365402.5:p.Pro304Thr
ENST00000376228.9:c.910C>A ENSP00000365402.5:p.Pro304Thr
ENST00000376237.8:c.*497C>A ENSP00000365412.4:n.*497C>A
ENST00000383329.7:c.910C>A ENSP00000372819.3:p.Pro304Thr
ENST00000470363.5:n.228C>A
ENST00000487245.5:n.1269C>A
NM_002117.5:c.910C>A NP_002108.4:p.Pro304Thr
NM_002117.6:c.910C>A MANE Select NP_002108.4:p.Pro304Thr
Search 100 bp 5'
Search 100 bp 3'