Canonical Allele Identifier: CA3403703

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs767034234
• ExAC: 5:131676288 T / A
• gnomAD v2: 5-131676288-T-A
• gnomAD v4: 5-132340595-T-A
• MyVariant Identifiers: chr5:g.131676288T>A (hg19) ; chr5:g.132340595T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340595T>A , CM000667.2:g.132340595T>A	GRCh38
NC_000005.9:g.131676288T>A , CM000667.1:g.131676288T>A	GRCh37
NC_000005.8:g.131704187T>A	NCBI36
NG_012129.1:g.51144T>A
NG_012129.2:g.51144T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1475T>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Val492Asp
ENST00000200652.3:c.1475T>A (SLC22A4)	ENSP00000200652.3:p.Val492Asp
NM_003059.2:c.1475T>A (SLC22A4)	NP_003050.2:p.Val492Asp
NR_110997.1:n.561-5669A>T (MIR3936HG)
XM_006714675.2:c.947T>A (SLC22A4)	XP_006714738.1:p.Val316Asp
XM_011543589.1:c.1199T>A (SLC22A4)	XP_011541891.1:p.Val400Asp
XM_006714675.4:c.947T>A (SLC22A4)	XP_006714738.1:p.Val316Asp
XM_011543589.2:c.1199T>A (SLC22A4)	XP_011541891.1:p.Val400Asp
XM_017009776.1:c.947T>A (SLC22A4)	XP_016865265.1:p.Val316Asp
NM_003059.3:c.1475T>A (SLC22A4) MANE Select	NP_003050.2:p.Val492Asp