Canonical Allele Identifier: CA1087425714
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2113908656
gnomAD v3: 6-31270966-A-T
gnomAD v4: 6-31270966-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270966A>T , CM000668.2:g.31270966A>T GRCh38
NC_000006.11:g.31238743A>T , CM000668.1:g.31238743A>T GRCh37
NC_000006.10:g.31346722A>T NCBI36
NG_029422.2:g.6166T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+107T>A MANE Select ENSP00000365402.5:n.619+107T>A
ENST00000376228.9:c.619+107T>A ENSP00000365402.5:n.619+107T>A
ENST00000376237.8:c.*206+107T>A ENSP00000365412.4:n.*206+107T>A
ENST00000383329.7:c.619+107T>A ENSP00000372819.3:n.619+107T>A
ENST00000415537.1:c.617+107T>A
ENST00000487245.5:n.978+107T>A
ENST00000495835.1:n.808+107T>A
NM_002117.5:c.619+107T>A NP_002108.4:n.619+107T>A
NM_002117.6:c.619+107T>A MANE Select NP_002108.4:n.619+107T>A
Search 100 bp 5'
Search 100 bp 3'