Canonical Allele Identifier: CA3403448

Gene: SLC22A4 MIR3936HG

Linked Data

• ClinVar Variation Id: 2026472
• ClinVar RCV Id: RCV002871375
• dbSNP Id: rs754580524
• ExAC: 5:131649400 T / A
• gnomAD v2: 5-131649400-T-A
• gnomAD v4: 5-132313707-T-A
• MyVariant Identifiers: chr5:g.131649400T>A (hg19) ; chr5:g.132313707T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313707T>A , CM000667.2:g.132313707T>A	GRCh38
NC_000005.9:g.131649400T>A , CM000667.1:g.131649400T>A	GRCh37
NC_000005.8:g.131677299T>A	NCBI36
NG_012129.1:g.24256T>A
NG_012129.2:g.24256T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.591T>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr197=
ENST00000200652.3:c.591T>A (SLC22A4)	ENSP00000200652.3:p.Thr197=
ENST00000491257.1:n.395T>A (SLC22A4)
NM_003059.2:c.591T>A (SLC22A4)	NP_003050.2:p.Thr197=
NR_110997.1:n.825-1454A>T (MIR3936HG)
XM_006714675.2:c.63T>A (SLC22A4)	XP_006714738.1:p.Thr21=
XM_011543589.1:c.487T>A (SLC22A4)	XP_011541891.1:p.Cys163Ser
XM_006714675.4:c.63T>A (SLC22A4)	XP_006714738.1:p.Thr21=
XM_011543589.2:c.487T>A (SLC22A4)	XP_011541891.1:p.Cys163Ser
XM_017009776.1:c.63T>A (SLC22A4)	XP_016865265.1:p.Thr21=
NM_003059.3:c.591T>A (SLC22A4) MANE Select	NP_003050.2:p.Thr197=