Canonical Allele Identifier: CA446328458

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1750247181
• MyVariant Identifiers: chr5:g.131649328C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313635C>T , CM000667.2:g.132313635C>T	GRCh38
NC_000005.9:g.131649328C>T , CM000667.1:g.131649328C>T	GRCh37
NC_000005.8:g.131677227C>T	NCBI36
NG_012129.1:g.24184C>T
NG_012129.2:g.24184C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.519C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Leu173=
ENST00000200652.3:c.519C>T (SLC22A4)	ENSP00000200652.3:p.Leu173=
ENST00000491257.1:n.323C>T (SLC22A4)
NM_003059.2:c.519C>T (SLC22A4)	NP_003050.2:p.Leu173=
NR_110997.1:n.825-1382G>A (MIR3936HG)
XM_006714675.2:c.-10C>T (SLC22A4)	XP_006714738.1:n.-10C>T
XM_011543589.1:c.415C>T (SLC22A4)	XP_011541891.1:p.Leu139Phe
XM_006714675.4:c.-10C>T (SLC22A4)	XP_006714738.1:n.-10C>T
XM_011543589.2:c.415C>T (SLC22A4)	XP_011541891.1:p.Leu139Phe
XM_017009776.1:c.-10C>T (SLC22A4)	XP_016865265.1:n.-10C>T
NM_003059.3:c.519C>T (SLC22A4) MANE Select	NP_003050.2:p.Leu173=