Canonical Allele Identifier: CA15422218
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs2735102
gnomAD v2: 6-29912925-A-G
gnomAD v3: 6-29945148-A-G
gnomAD v4: 6-29945148-A-G
MyVariant Identifiers: chr6:g.29912925A>G (hg19) chr6:g.29945148A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945148A>G , CM000668.2:g.29945148A>G GRCh38
NC_000006.11:g.29912925A>G , CM000668.1:g.29912925A>G GRCh37
NC_000006.10:g.30020904A>G NCBI36
NG_029217.2:g.7684A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.928+57A>G ENSP00000492789.2:n.928+57A>G
ENST00000706892.1:n.2500A>G
ENST00000706893.1:c.*29+57A>G ENSP00000516609.1:n.*29+57A>G
ENST00000706894.1:c.1045+57A>G ENSP00000516610.1:n.1045+57A>G
ENST00000706895.1:n.1865+57A>G
ENST00000706896.1:n.2341+57A>G
ENST00000706897.1:n.1763+57A>G
ENST00000706898.1:c.1063+57A>G ENSP00000516611.1:n.1063+57A>G
ENST00000706899.1:n.1899+57A>G
ENST00000706900.1:c.961+57A>G ENSP00000516617.1:n.961+57A>G
ENST00000706901.1:c.1045+57A>G ENSP00000516612.1:n.1045+57A>G
ENST00000706902.1:c.1045+57A>G ENSP00000516613.1:n.1045+57A>G
ENST00000706903.1:c.1045+57A>G ENSP00000516614.1:n.1045+57A>G
ENST00000706904.1:c.1045+57A>G ENSP00000516615.1:n.1045+57A>G
ENST00000706905.1:c.1045+57A>G ENSP00000516616.1:n.1045+57A>G
ENST00000376809.10:c.1045+57A>G MANE Select ENSP00000366005.5:n.1045+57A>G
ENST00000638375.1:c.928+57A>G ENSP00000492789.1:n.928+57A>G
ENST00000376802.2:c.896-303A>G ENSP00000365998.2:n.896-303A>G
ENST00000376806.9:c.1063+57A>G ENSP00000366002.5:n.1063+57A>G
ENST00000376809.9:c.1045+57A>G ENSP00000366005.5:n.1045+57A>G
ENST00000396634.5:c.1045+57A>G ENSP00000379873.1:n.1045+57A>G
ENST00000461903.1:n.1304+57A>G
ENST00000479320.5:n.1286+57A>G
ENST00000495183.5:n.1284+57A>G
ENST00000496081.5:n.1304+57A>G
NM_002116.7:c.1045+57A>G NP_002107.3:n.1045+57A>G
NM_002116.8:c.1045+57A>G MANE Select NP_002107.3:n.1045+57A>G
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