Canonical Allele Identifier: CA3693203
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs41563617
ExAC: 6:29910799 G / A
gnomAD v2: 6-29910799-G-A
gnomAD v3: 6-29943022-G-A
gnomAD v4: 6-29943022-G-A
MyVariant Identifiers: chr6:g.29910799G>A (hg19) chr6:g.29943022G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943022G>A , CM000668.2:g.29943022G>A GRCh38
NC_000006.11:g.29910799G>A , CM000668.1:g.29910799G>A GRCh37
NC_000006.10:g.30018778G>A NCBI36
NG_029217.2:g.5557G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.339G>A ENSP00000492789.2:p.Glu113=
ENST00000706892.1:n.615G>A
ENST00000706893.1:c.339G>A ENSP00000516609.1:p.Glu113=
ENST00000706894.1:c.339G>A ENSP00000516610.1:p.Glu113=
ENST00000706895.1:n.615G>A
ENST00000706896.1:n.615G>A
ENST00000706897.1:n.615G>A
ENST00000706898.1:c.339G>A ENSP00000516611.1:p.Glu113=
ENST00000706899.1:n.615G>A
ENST00000706900.1:c.255G>A ENSP00000516617.1:p.Glu85=
ENST00000706901.1:c.339G>A ENSP00000516612.1:p.Glu113=
ENST00000706902.1:c.339G>A ENSP00000516613.1:p.Glu113=
ENST00000706903.1:c.339G>A ENSP00000516614.1:p.Glu113=
ENST00000706904.1:c.339G>A ENSP00000516615.1:p.Glu113=
ENST00000706905.1:c.339G>A ENSP00000516616.1:p.Glu113=
ENST00000376809.10:c.339G>A MANE Select ENSP00000366005.5:p.Glu113=
ENST00000638375.1:c.339G>A ENSP00000492789.1:p.Glu113=
ENST00000376802.2:c.339G>A ENSP00000365998.2:p.Glu113=
ENST00000376806.9:c.339G>A ENSP00000366002.5:p.Glu113=
ENST00000376809.9:c.339G>A ENSP00000366005.5:p.Glu113=
ENST00000396634.5:c.339G>A ENSP00000379873.1:p.Glu113=
ENST00000429656.1:n.46C>T
ENST00000461903.1:n.339G>A
ENST00000479320.5:n.339G>A
ENST00000495183.5:n.341G>A
ENST00000496081.5:n.177+168G>A
NM_002116.7:c.339G>A NP_002107.3:p.Glu113=
NM_002116.8:c.339G>A MANE Select NP_002107.3:p.Glu113=
Search 100 bp 5'
Search 100 bp 3'