Canonical Allele Identifier: CA413655968
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641665C>A (hg19) chrX:g.74421830C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421830C>A , CM000685.2:g.74421830C>A GRCh38
NC_000023.10:g.73641665C>A , CM000685.1:g.73641665C>A GRCh37
NC_000023.9:g.73558390C>A NCBI36
NG_011641.1:g.5581C>A
NG_011641.2:g.5581C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.193C>A MANE Select ENSP00000465734.1:p.Pro65Thr
ENST00000587091.5:c.193C>A ENSP00000465734.1:p.Pro65Thr
NM_006517.4:c.193C>A NP_006508.2:p.Pro65Thr
XM_005262294.1:c.193C>A XP_005262351.1:p.Pro65Thr
XM_011531015.1:c.193C>A XP_011529317.1:p.Pro65Thr
NM_006517.5:c.193C>A MANE Select NP_006508.2:p.Pro65Thr
Search 100 bp 5'
Search 100 bp 3'