Canonical Allele Identifier: CA413655878

Gene: SLC16A2

Linked Data

• dbSNP Id: rs2147833939
• MyVariant Identifiers: chrX:g.73641621A>C (hg19) ; chrX:g.74421786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421786A>C , CM000685.2:g.74421786A>C	GRCh38
NC_000023.10:g.73641621A>C , CM000685.1:g.73641621A>C	GRCh37
NC_000023.9:g.73558346A>C	NCBI36
NG_011641.1:g.5537A>C
NG_011641.2:g.5537A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.149A>C MANE Select	ENSP00000465734.1:p.Glu50Ala
ENST00000587091.5:c.149A>C	ENSP00000465734.1:p.Glu50Ala
NM_006517.4:c.149A>C	NP_006508.2:p.Glu50Ala
XM_005262294.1:c.149A>C	XP_005262351.1:p.Glu50Ala
XM_011531015.1:c.149A>C	XP_011529317.1:p.Glu50Ala
NM_006517.5:c.149A>C MANE Select	NP_006508.2:p.Glu50Ala