Canonical Allele Identifier: CA3693755

Gene: HLA-A

Linked Data

• dbSNP Id: rs2975055
• ExAC: 6:29913191 T / C
• gnomAD v2: 6-29913191-T-C
• gnomAD v3: 6-29945414-T-C
• gnomAD v4: 6-29945414-T-C
• MyVariant Identifiers: chr6:g.29913191T>C (hg19) ; chr6:g.29945414T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945414T>C , CM000668.2:g.29945414T>C	GRCh38
NC_000006.11:g.29913191T>C , CM000668.1:g.29913191T>C	GRCh37
NC_000006.10:g.30021170T>C	NCBI36
NG_029217.2:g.7950T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-37T>C	ENSP00000492789.2:n.977-37T>C
ENST00000706892.1:n.2766T>C
ENST00000706893.1:c.*78-37T>C	ENSP00000516609.1:n.*78-37T>C
ENST00000706894.1:c.*41T>C	ENSP00000516610.1:n.*41T>C
ENST00000706895.1:n.2046T>C
ENST00000706896.1:n.2390-37T>C
ENST00000706897.1:n.1812-37T>C
ENST00000706898.1:c.1112-37T>C	ENSP00000516611.1:n.1112-37T>C
ENST00000706899.1:n.1948-37T>C
ENST00000706900.1:c.1010-37T>C	ENSP00000516617.1:n.1010-37T>C
ENST00000706901.1:c.1094-37T>C	ENSP00000516612.1:n.1094-37T>C
ENST00000706902.1:c.1093+133T>C	ENSP00000516613.1:n.1093+133T>C
ENST00000706903.1:c.1094-37T>C	ENSP00000516614.1:n.1094-37T>C
ENST00000706904.1:c.1093+133T>C	ENSP00000516615.1:n.1093+133T>C
ENST00000706905.1:c.1094-37T>C	ENSP00000516616.1:n.1094-37T>C
ENST00000376809.10:c.1094-37T>C MANE Select	ENSP00000366005.5:n.1094-37T>C
ENST00000376802.2:c.896-37T>C	ENSP00000365998.2:n.896-37T>C
ENST00000376806.9:c.1112-37T>C	ENSP00000366002.5:n.1112-37T>C
ENST00000376809.9:c.1094-37T>C	ENSP00000366005.5:n.1094-37T>C
ENST00000396634.5:c.1094-37T>C	ENSP00000379873.1:n.1094-37T>C
ENST00000495183.5:n.1333-37T>C
ENST00000496081.5:n.1353-37T>C
NM_002116.7:c.1094-37T>C	NP_002107.3:n.1094-37T>C
NM_002116.8:c.1094-37T>C MANE Select	NP_002107.3:n.1094-37T>C