Canonical Allele Identifier: CA413656133
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641746T>A (hg19) chrX:g.74421911T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421911T>A , CM000685.2:g.74421911T>A GRCh38
NC_000023.10:g.73641746T>A , CM000685.1:g.73641746T>A GRCh37
NC_000023.9:g.73558471T>A NCBI36
NG_011641.1:g.5662T>A
NG_011641.2:g.5662T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.274T>A MANE Select ENSP00000465734.1:p.Phe92Ile
ENST00000636771.1:c.20T>A
ENST00000587091.5:c.274T>A ENSP00000465734.1:p.Phe92Ile
NM_006517.4:c.274T>A NP_006508.2:p.Phe92Ile
XM_005262294.1:c.274T>A XP_005262351.1:p.Phe92Ile
XM_011531015.1:c.274T>A XP_011529317.1:p.Phe92Ile
NM_006517.5:c.274T>A MANE Select NP_006508.2:p.Phe92Ile
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