Canonical Allele Identifier: CA136017383
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs549928301
gnomAD v2: 6-29909769-A-C
gnomAD v3: 6-29941992-A-C
gnomAD v4: 6-29941992-A-C
MyVariant Identifiers: chr6:g.29909769A>C (hg19) chr6:g.29909769_29909772delinsCAAC (hg19) chr6:g.29941992A>C (hg38) chr6:g.29941992_29941995delinsCAAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29941992A>C , CM000668.2:g.29941992A>C GRCh38
NC_000006.11:g.29909769A>C , CM000668.1:g.29909769A>C GRCh37
NC_000006.10:g.30017748A>C NCBI36
NG_029217.2:g.4530A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706892.1:n.22A>C
ENST00000706893.1:c.-255A>C ENSP00000516609.1:n.-255A>C
ENST00000706894.1:c.-255A>C ENSP00000516610.1:n.-255A>C
ENST00000706895.1:n.22A>C
ENST00000706896.1:n.22A>C
ENST00000706897.1:n.22A>C
ENST00000706898.1:c.-255A>C ENSP00000516611.1:n.-255A>C
ENST00000706899.1:n.22A>C
ENST00000706901.1:c.-255A>C ENSP00000516612.1:n.-255A>C
ENST00000706902.1:c.-255A>C ENSP00000516613.1:n.-255A>C
ENST00000706903.1:c.-255A>C ENSP00000516614.1:n.-255A>C
ENST00000706904.1:c.-255A>C ENSP00000516615.1:n.-255A>C
ENST00000396634.5:c.-255A>C ENSP00000379873.1:n.-255A>C
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