Canonical Allele Identifier: CA15448594
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs2975050 rs2113371989 rs2113372005 rs2113372031 rs2113372040 rs2113372050 rs2113372067 rs2113372088 rs2113372107 rs2113372123
gnomAD v2: 6-29913817-C-T
gnomAD v3: 6-29946040-C-T
gnomAD v4: 6-29946040-C-T
MyVariant Identifiers: chr6:g.29913817C>T (hg19) chr6:g.29946040C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29946040C>T , CM000668.2:g.29946040C>T GRCh38
NC_000006.11:g.29913817C>T , CM000668.1:g.29913817C>T GRCh37
NC_000006.10:g.30021796C>T NCBI36
NG_029217.2:g.8576C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*585C>T ENSP00000516612.1:n.*585C>T
ENST00000706902.1:c.1093+759C>T ENSP00000516613.1:n.1093+759C>T
ENST00000706903.1:c.*124+461C>T ENSP00000516614.1:n.*124+461C>T
ENST00000706904.1:c.1093+759C>T ENSP00000516615.1:n.1093+759C>T
ENST00000706905.1:c.*585C>T ENSP00000516616.1:n.*585C>T
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