Canonical Allele Identifier: CA446328385

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs371708747
• MyVariant Identifiers: chr5:g.131649314A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313621A>C , CM000667.2:g.132313621A>C	GRCh38
NC_000005.9:g.131649314A>C , CM000667.1:g.131649314A>C	GRCh37
NC_000005.8:g.131677213A>C	NCBI36
NG_012129.1:g.24170A>C
NG_012129.2:g.24170A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.505A>C (SLC22A4) MANE Select	ENSP00000200652.3:p.Arg169=
ENST00000200652.3:c.505A>C (SLC22A4)	ENSP00000200652.3:p.Arg169=
ENST00000491257.1:n.309A>C (SLC22A4)
NM_003059.2:c.505A>C (SLC22A4)	NP_003050.2:p.Arg169=
NR_110997.1:n.825-1368T>G (MIR3936HG)
XM_006714675.2:c.-24A>C (SLC22A4)	XP_006714738.1:n.-24A>C
XM_011543589.1:c.401A>C (SLC22A4)	XP_011541891.1:p.Gln134Pro
XM_006714675.4:c.-24A>C (SLC22A4)	XP_006714738.1:n.-24A>C
XM_011543589.2:c.401A>C (SLC22A4)	XP_011541891.1:p.Gln134Pro
XM_017009776.1:c.-24A>C (SLC22A4)	XP_016865265.1:n.-24A>C
NM_003059.3:c.505A>C (SLC22A4) MANE Select	NP_003050.2:p.Arg169=