Canonical Allele Identifier: CA360803855

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649329T>G (hg19) ; chr5:g.132313636T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313636T>G , CM000667.2:g.132313636T>G	GRCh38
NC_000005.9:g.131649329T>G , CM000667.1:g.131649329T>G	GRCh37
NC_000005.8:g.131677228T>G	NCBI36
NG_012129.1:g.24185T>G
NG_012129.2:g.24185T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.520T>G (SLC22A4) MANE Select	ENSP00000200652.3:p.Phe174Val
ENST00000200652.3:c.520T>G (SLC22A4)	ENSP00000200652.3:p.Phe174Val
ENST00000491257.1:n.324T>G (SLC22A4)
NM_003059.2:c.520T>G (SLC22A4)	NP_003050.2:p.Phe174Val
NR_110997.1:n.825-1383A>C (MIR3936HG)
XM_006714675.2:c.-9T>G (SLC22A4)	XP_006714738.1:n.-9T>G
XM_011543589.1:c.416T>G (SLC22A4)	XP_011541891.1:p.Leu139Arg
XM_006714675.4:c.-9T>G (SLC22A4)	XP_006714738.1:n.-9T>G
XM_011543589.2:c.416T>G (SLC22A4)	XP_011541891.1:p.Leu139Arg
XM_017009776.1:c.-9T>G (SLC22A4)	XP_016865265.1:n.-9T>G
NM_003059.3:c.520T>G (SLC22A4) MANE Select	NP_003050.2:p.Phe174Val