Canonical Allele Identifier: CA3710858
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs202001134
gnomAD v2: 6-31239371-C-A
gnomAD v3: 6-31271594-C-A
gnomAD v4: 6-31271594-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271594C>A , CM000668.2:g.31271594C>A GRCh38
NC_000006.11:g.31239371C>A , CM000668.1:g.31239371C>A GRCh37
NC_000006.10:g.31347350C>A NCBI36
NG_029422.2:g.5538G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+5G>T MANE Select ENSP00000365402.5:n.343+5G>T
ENST00000376228.9:c.343+5G>T ENSP00000365402.5:n.343+5G>T
ENST00000376237.8:c.343+5G>T ENSP00000365412.4:n.343+5G>T
ENST00000383329.7:c.343+5G>T ENSP00000372819.3:n.343+5G>T
ENST00000415537.1:c.341+5G>T
ENST00000484378.1:n.367G>T
ENST00000487245.5:n.457G>T
ENST00000495835.1:n.532+5G>T
NM_002117.5:c.343+5G>T NP_002108.4:n.343+5G>T
NM_002117.6:c.343+5G>T MANE Select NP_002108.4:n.343+5G>T