Canonical Allele Identifier: CA3693773
Gene: HLA-A HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.29945489G>T
GRCh37 chr6:g.29913266G>T
gnomAD v2:
6:29913266 G / T
gnomAD v3:
6:29945489 G / T
gnomAD v4:
chr6-29945489-G-T
Joint Max Group AF 0.10960153 (AFR)
Genomes Max Group AF 0.14106123 (AFR)
Exomes Max Group AF 0.07660726 (EAS)
dbSNP:
1061156
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945489G>T , CM000668.2:g.29945489G>T GRCh38
NC_000006.11:g.29913266G>T , CM000668.1:g.29913266G>T GRCh37
NC_000006.10:g.30021245G>T NCBI36
NG_029217.2:g.8025G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1015G>T ENSP00000492789.2:n.1015G>T
ENST00000706892.1:n.2841G>T
ENST00000706893.1:c.*116G>T ENSP00000516609.1:n.*116G>T
ENST00000706894.1:c.*116G>T ENSP00000516610.1:n.*116G>T
ENST00000706895.1:n.2121G>T
ENST00000706896.1:n.2428G>T
ENST00000706897.1:n.1850G>T
ENST00000706898.1:c.*34G>T ENSP00000516611.1:n.*34G>T
ENST00000706899.1:n.1986G>T
ENST00000706900.1:c.*34G>T ENSP00000516617.1:n.*34G>T
ENST00000706901.1:c.*34G>T ENSP00000516612.1:n.*34G>T
ENST00000706902.1:c.1093+208G>T ENSP00000516613.1:n.1093+208G>T
ENST00000706903.1:c.*34G>T ENSP00000516614.1:n.*34G>T
ENST00000706904.1:c.1093+208G>T ENSP00000516615.1:n.1093+208G>T
ENST00000706905.1:c.*34G>T ENSP00000516616.1:n.*34G>T
ENST00000376809.10:c.*34G>T MANE Select ENSP00000366005.5:n.*34G>T
ENST00000376802.2:c.*34G>T ENSP00000365998.2:n.*34G>T
ENST00000376806.9:c.*34G>T ENSP00000366002.5:n.*34G>T
ENST00000376809.9:c.*34G>T ENSP00000366005.5:n.*34G>T
ENST00000396634.5:c.*34G>T ENSP00000379873.1:n.*34G>T
ENST00000495183.5:n.1371G>T
ENST00000496081.5:n.1391G>T
NM_002116.7:c.*34G>T NP_002107.3:n.*34G>T
NM_002116.8:c.*34G>T MANE Select NP_002107.3:n.*34G>T
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