Canonical Allele Identifier: CA2437472685

Gene: SLC16A2

Linked Data

• dbSNP Id: rs1569281220

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74422072G>A , CM000685.2:g.74422072G>A	GRCh38
NC_000023.10:g.73641907G>A , CM000685.1:g.73641907G>A	GRCh37
NC_000023.9:g.73558632G>A	NCBI36
NG_011641.1:g.5823G>A
NG_011641.2:g.5823G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.430+5G>A MANE Select	ENSP00000465734.1:n.430+5G>A
ENST00000636771.1:c.176+5G>A
ENST00000587091.5:c.430+5G>A	ENSP00000465734.1:n.430+5G>A
NM_006517.4:c.430+5G>A	NP_006508.2:n.430+5G>A
XM_005262294.1:c.430+5G>A	XP_005262351.1:n.430+5G>A
XM_011531015.1:c.430+5G>A	XP_011529317.1:n.430+5G>A
NM_006517.5:c.430+5G>A MANE Select	NP_006508.2:n.430+5G>A