Canonical Allele Identifier: CA136018960
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474352
gnomAD v4: 6-29942779-C-G
MyVariant Identifiers: chr6:g.29910556C>G (hg19) chr6:g.29942779C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942779C>G , CM000668.2:g.29942779C>G GRCh38
NC_000006.11:g.29910556C>G , CM000668.1:g.29910556C>G GRCh37
NC_000006.10:g.30018535C>G NCBI36
NG_029217.2:g.5314C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.96C>G ENSP00000492789.2:p.Phe32Leu
ENST00000706892.1:n.372C>G
ENST00000706893.1:c.96C>G ENSP00000516609.1:p.Phe32Leu
ENST00000706894.1:c.96C>G ENSP00000516610.1:p.Phe32Leu
ENST00000706895.1:n.372C>G
ENST00000706896.1:n.372C>G
ENST00000706897.1:n.372C>G
ENST00000706898.1:c.96C>G ENSP00000516611.1:p.Phe32Leu
ENST00000706899.1:n.372C>G
ENST00000706900.1:c.12C>G ENSP00000516617.1:p.Phe4Leu
ENST00000706901.1:c.96C>G ENSP00000516612.1:p.Phe32Leu
ENST00000706902.1:c.96C>G ENSP00000516613.1:p.Phe32Leu
ENST00000706903.1:c.96C>G ENSP00000516614.1:p.Phe32Leu
ENST00000706904.1:c.96C>G ENSP00000516615.1:p.Phe32Leu
ENST00000706905.1:c.96C>G ENSP00000516616.1:p.Phe32Leu
ENST00000376809.10:c.96C>G MANE Select ENSP00000366005.5:p.Phe32Leu
ENST00000638375.1:c.96C>G ENSP00000492789.1:p.Phe32Leu
ENST00000376802.2:c.96C>G ENSP00000365998.2:p.Phe32Leu
ENST00000376806.9:c.96C>G ENSP00000366002.5:p.Phe32Leu
ENST00000376809.9:c.96C>G ENSP00000366005.5:p.Phe32Leu
ENST00000396634.5:c.96C>G ENSP00000379873.1:p.Phe32Leu
ENST00000429656.1:n.289G>C
ENST00000461903.1:n.96C>G
ENST00000479320.5:n.96C>G
ENST00000495183.5:n.98C>G
ENST00000496081.5:n.102C>G
NM_002116.7:c.96C>G NP_002107.3:p.Phe32Leu
NM_002116.8:c.96C>G MANE Select NP_002107.3:p.Phe32Leu
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