Canonical Allele Identifier: CA136024029
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474575
gnomAD v4: 6-29943520-G-C
MyVariant Identifiers: chr6:g.29911297G>C (hg19) chr6:g.29943520G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943520G>C , CM000668.2:g.29943520G>C GRCh38
NC_000006.11:g.29911297G>C , CM000668.1:g.29911297G>C GRCh37
NC_000006.10:g.30019276G>C NCBI36
NG_029217.2:g.6055G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.596G>C ENSP00000492789.2:p.Gly199Ala
ENST00000706892.1:n.872G>C
ENST00000706893.1:c.596G>C ENSP00000516609.1:p.Gly199Ala
ENST00000706894.1:c.596G>C ENSP00000516610.1:p.Gly199Ala
ENST00000706895.1:n.872G>C
ENST00000706896.1:n.872G>C
ENST00000706897.1:n.872G>C
ENST00000706898.1:c.596G>C ENSP00000516611.1:p.Gly199Ala
ENST00000706899.1:n.872G>C
ENST00000706900.1:c.512G>C ENSP00000516617.1:p.Gly171Ala
ENST00000706901.1:c.596G>C ENSP00000516612.1:p.Gly199Ala
ENST00000706902.1:c.596G>C ENSP00000516613.1:p.Gly199Ala
ENST00000706903.1:c.596G>C ENSP00000516614.1:p.Gly199Ala
ENST00000706904.1:c.596G>C ENSP00000516615.1:p.Gly199Ala
ENST00000706905.1:c.596G>C ENSP00000516616.1:p.Gly199Ala
ENST00000376809.10:c.596G>C MANE Select ENSP00000366005.5:p.Gly199Ala
ENST00000638375.1:c.596G>C ENSP00000492789.1:p.Gly199Ala
ENST00000376802.2:c.596G>C ENSP00000365998.2:p.Gly199Ala
ENST00000376806.9:c.596G>C ENSP00000366002.5:p.Gly199Ala
ENST00000376809.9:c.596G>C ENSP00000366005.5:p.Gly199Ala
ENST00000396634.5:c.596G>C ENSP00000379873.1:p.Gly199Ala
ENST00000461903.1:n.837G>C
ENST00000479320.5:n.837G>C
ENST00000495183.5:n.839G>C
ENST00000496081.5:n.413G>C
NM_002116.7:c.596G>C NP_002107.3:p.Gly199Ala
NM_002116.8:c.596G>C MANE Select NP_002107.3:p.Gly199Ala
Search 100 bp 5'
Search 100 bp 3'