Canonical Allele Identifier: CA136024255
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474601
gnomAD v3: 6-29943714-T-G
gnomAD v4: 6-29943714-T-G
MyVariant Identifiers: chr6:g.29911491T>G (hg19) chr6:g.29943714T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943714T>G , CM000668.2:g.29943714T>G GRCh38
NC_000006.11:g.29911491T>G , CM000668.1:g.29911491T>G GRCh37
NC_000006.10:g.30019470T>G NCBI36
NG_029217.2:g.6250T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.619+171T>G ENSP00000492789.2:n.619+171T>G
ENST00000706892.1:n.1066T>G
ENST00000706893.1:c.619+171T>G ENSP00000516609.1:n.619+171T>G
ENST00000706894.1:c.619+171T>G ENSP00000516610.1:n.619+171T>G
ENST00000706895.1:n.895+171T>G
ENST00000706896.1:n.1066T>G
ENST00000706897.1:n.895+171T>G
ENST00000706898.1:c.619+171T>G ENSP00000516611.1:n.619+171T>G
ENST00000706899.1:n.1066T>G
ENST00000706900.1:c.535+171T>G ENSP00000516617.1:n.535+171T>G
ENST00000706901.1:c.619+171T>G ENSP00000516612.1:n.619+171T>G
ENST00000706902.1:c.619+171T>G ENSP00000516613.1:n.619+171T>G
ENST00000706903.1:c.619+171T>G ENSP00000516614.1:n.619+171T>G
ENST00000706904.1:c.619+171T>G ENSP00000516615.1:n.619+171T>G
ENST00000706905.1:c.619+171T>G ENSP00000516616.1:n.619+171T>G
ENST00000376809.10:c.619+171T>G MANE Select ENSP00000366005.5:n.619+171T>G
ENST00000638375.1:c.619+171T>G ENSP00000492789.1:n.619+171T>G
ENST00000376802.2:c.619+171T>G ENSP00000365998.2:n.619+171T>G
ENST00000376806.9:c.619+171T>G ENSP00000366002.5:n.619+171T>G
ENST00000376809.9:c.619+171T>G ENSP00000366005.5:n.619+171T>G
ENST00000396634.5:c.619+171T>G ENSP00000379873.1:n.619+171T>G
ENST00000461903.1:n.860+171T>G
ENST00000479320.5:n.860+171T>G
ENST00000495183.5:n.862+171T>G
ENST00000496081.5:n.436+171T>G
NM_002116.7:c.619+171T>G NP_002107.3:n.619+171T>G
NM_002116.8:c.619+171T>G MANE Select NP_002107.3:n.619+171T>G
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