Canonical Allele Identifier: CA136017607

Gene: HLA-A

Linked Data

• dbSNP Id: rs529413410
• gnomAD v2: 6-29910112-T-C
• gnomAD v3: 6-29942335-T-C
• gnomAD v4: 6-29942335-T-C
• MyVariant Identifiers: chr6:g.29910112T>C (hg19) ; chr6:g.29942335T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942335T>C , CM000668.2:g.29942335T>C	GRCh38
NC_000006.11:g.29910112T>C , CM000668.1:g.29910112T>C	GRCh37
NC_000006.10:g.30018091T>C	NCBI36
NG_029217.2:g.4870T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.127-69T>C
ENST00000706893.1:c.-150-69T>C	ENSP00000516609.1:n.-150-69T>C
ENST00000706894.1:c.-150-69T>C	ENSP00000516610.1:n.-150-69T>C
ENST00000706895.1:n.127-69T>C
ENST00000706896.1:n.127-69T>C
ENST00000706897.1:n.127-69T>C
ENST00000706898.1:c.-150-69T>C	ENSP00000516611.1:n.-150-69T>C
ENST00000706899.1:n.127-69T>C
ENST00000706901.1:c.-150-69T>C	ENSP00000516612.1:n.-150-69T>C
ENST00000706902.1:c.-150-69T>C	ENSP00000516613.1:n.-150-69T>C
ENST00000706903.1:c.-150-69T>C	ENSP00000516614.1:n.-150-69T>C
ENST00000706904.1:c.-150-69T>C	ENSP00000516615.1:n.-150-69T>C
ENST00000706905.1:c.-219T>C	ENSP00000516616.1:n.-219T>C
ENST00000376806.9:c.-219T>C	ENSP00000366002.5:n.-219T>C
ENST00000396634.5:c.-150-69T>C	ENSP00000379873.1:n.-150-69T>C
ENST00000429656.1:n.733A>G