Canonical Allele Identifier: CA449370361
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29942254-C-A
MyVariant Identifiers: chr6:g.29910031C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29942254C>A , CM000668.2:g.29942254C>A GRCh38
NC_000006.11:g.29910031C>A , CM000668.1:g.29910031C>A GRCh37
NC_000006.10:g.30018010C>A NCBI36
NG_029217.2:g.4789C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706892.1:n.127-150C>A
ENST00000706893.1:c.-150-150C>A ENSP00000516609.1:n.-150-150C>A
ENST00000706894.1:c.-150-150C>A ENSP00000516610.1:n.-150-150C>A
ENST00000706895.1:n.127-150C>A
ENST00000706896.1:n.127-150C>A
ENST00000706897.1:n.127-150C>A
ENST00000706898.1:c.-150-150C>A ENSP00000516611.1:n.-150-150C>A
ENST00000706899.1:n.127-150C>A
ENST00000706901.1:c.-150-150C>A ENSP00000516612.1:n.-150-150C>A
ENST00000706902.1:c.-150-150C>A ENSP00000516613.1:n.-150-150C>A
ENST00000706903.1:c.-150-150C>A ENSP00000516614.1:n.-150-150C>A
ENST00000706904.1:c.-150-150C>A ENSP00000516615.1:n.-150-150C>A
ENST00000376806.9:c.-300C>A ENSP00000366002.5:n.-300C>A
ENST00000396634.5:c.-150-150C>A ENSP00000379873.1:n.-150-150C>A
ENST00000429656.1:n.814G>T