Canonical Allele Identifier: CA15448595

Gene: HLA-A

Linked Data

• dbSNP Id: rs9404954 ; rs2113372660 ; rs2113372680 ; rs2113372719 ; rs2113372732 ; rs2113372750 ; rs2113372763 ; rs2113372774 ; rs2113372799
• gnomAD v2: 6-29913881-T-C
• gnomAD v3: 6-29946104-T-C
• gnomAD v4: 6-29946104-T-C
• MyVariant Identifiers: chr6:g.29913881T>C (hg19) ; chr6:g.29946104T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29946104T>C , CM000668.2:g.29946104T>C	GRCh38
NC_000006.11:g.29913881T>C , CM000668.1:g.29913881T>C	GRCh37
NC_000006.10:g.30021860T>C	NCBI36
NG_029217.2:g.8640T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706901.1:c.*649T>C	ENSP00000516612.1:n.*649T>C
ENST00000706902.1:c.1093+823T>C	ENSP00000516613.1:n.1093+823T>C
ENST00000706903.1:c.*124+525T>C	ENSP00000516614.1:n.*124+525T>C
ENST00000706904.1:c.1093+823T>C	ENSP00000516615.1:n.1093+823T>C
ENST00000706905.1:c.*649T>C	ENSP00000516616.1:n.*649T>C