Canonical Allele Identifier: CA363568622
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1762737662
MyVariant Identifiers: chr6:g.32411151T>C (hg19) chr6:g.32443374T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443374T>C , CM000668.2:g.32443374T>C GRCh38
NC_000006.11:g.32411151T>C , CM000668.1:g.32411151T>C GRCh37
NC_000006.10:g.32519129T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.518T>C MANE Select ENSP00000378786.2:p.Phe173Ser
ENST00000374982.5:c.443T>C ENSP00000364121.5:p.Phe148Ser
ENST00000395388.6:c.518T>C ENSP00000378786.2:p.Phe173Ser
NM_019111.4:c.518T>C NP_061984.2:p.Phe173Ser
NM_019111.5:c.518T>C MANE Select NP_061984.2:p.Phe173Ser
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