Canonical Allele Identifier: CA3710629
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41544520
ExAC: 6:31238507 C / T
gnomAD v2: 6-31238507-C-T
gnomAD v3: 6-31270730-C-T
gnomAD v4: 6-31270730-C-T
MyVariant Identifiers: chr6:g.31238507C>T (hg19) chr6:g.31270730C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270730C>T , CM000668.2:g.31270730C>T GRCh38
NC_000006.11:g.31238507C>T , CM000668.1:g.31238507C>T GRCh37
NC_000006.10:g.31346486C>T NCBI36
NG_029422.2:g.6402G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.620-245G>A MANE Select ENSP00000365402.5:n.620-245G>A
ENST00000376228.9:c.620-245G>A ENSP00000365402.5:n.620-245G>A
ENST00000376237.8:c.*207-245G>A ENSP00000365412.4:n.*207-245G>A
ENST00000383329.7:c.620-245G>A ENSP00000372819.3:n.620-245G>A
ENST00000415537.1:c.618-245G>A
ENST00000487245.5:n.979-245G>A
ENST00000495835.1:n.809-245G>A
NM_002117.5:c.620-245G>A NP_002108.4:n.620-245G>A
NM_002117.6:c.620-245G>A MANE Select NP_002108.4:n.620-245G>A
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