Canonical Allele Identifier: CA823770199
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1251375830
MyVariant Identifiers: chr6:g.29913930C>A (hg19) chr6:g.29946153C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29946153C>A , CM000668.2:g.29946153C>A GRCh38
NC_000006.11:g.29913930C>A , CM000668.1:g.29913930C>A GRCh37
NC_000006.10:g.30021909C>A NCBI36
NG_029217.2:g.8689C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*698C>A ENSP00000516612.1:n.*698C>A
ENST00000706902.1:c.1093+872C>A ENSP00000516613.1:n.1093+872C>A
ENST00000706903.1:c.*124+574C>A ENSP00000516614.1:n.*124+574C>A
ENST00000706904.1:c.1093+872C>A ENSP00000516615.1:n.1093+872C>A
ENST00000706905.1:c.*698C>A ENSP00000516616.1:n.*698C>A
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