Canonical Allele Identifier: CA449830846
Gene: HLA-DQA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32609774C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641997C>G , CM000668.2:g.32641997C>G GRCh38
NC_000006.11:g.32609774C>G , CM000668.1:g.32609774C>G GRCh37
NC_000006.10:g.32717752C>G NCBI36
NG_032876.1:g.9592C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343139.11:c.357C>G MANE Select ENSP00000339398.5:p.Ser119=
ENST00000343139.9:c.357C>G ENSP00000339398.5:p.Ser119=
ENST00000374949.2:c.357C>G ENSP00000364087.2:p.Ser119=
ENST00000395363.5:c.357C>G ENSP00000378767.1:p.Ser119=
ENST00000460633.1:n.385C>G
ENST00000482745.5:c.*1189C>G ENSP00000436546.1:n.*1189C>G
ENST00000496318.5:c.357C>G ENSP00000437302.1:p.Ser119=
NM_002122.3:c.357C>G NP_002113.2:p.Ser119=
XM_006715079.2:c.357C>G XP_006715142.1:p.Ser119=
XM_006715079.4:c.357C>G XP_006715142.1:p.Ser119=
XR_001744085.1:n.86+591G>C
NM_002122.5:c.357C>G MANE Select NP_002113.2:p.Ser119=