Canonical Allele Identifier: CA360803989
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1402254319

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313696G>A , CM000667.2:g.132313696G>A GRCh38
NC_000005.9:g.131649389G>A , CM000667.1:g.131649389G>A GRCh37
NC_000005.8:g.131677288G>A NCBI36
NG_012129.1:g.24245G>A
NG_012129.2:g.24245G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.580G>A (SLC22A4) MANE Select ENSP00000200652.3:p.Glu194Lys
ENST00000200652.3:c.580G>A (SLC22A4) ENSP00000200652.3:p.Glu194Lys
ENST00000491257.1:n.384G>A (SLC22A4)
NM_003059.2:c.580G>A (SLC22A4) NP_003050.2:p.Glu194Lys
NR_110997.1:n.825-1443C>T (MIR3936HG)
XM_006714675.2:c.52G>A (SLC22A4) XP_006714738.1:p.Glu18Lys
XM_011543589.1:c.476G>A (SLC22A4) XP_011541891.1:p.Gly159Glu
XM_006714675.4:c.52G>A (SLC22A4) XP_006714738.1:p.Glu18Lys
XM_011543589.2:c.476G>A (SLC22A4) XP_011541891.1:p.Gly159Glu
XM_017009776.1:c.52G>A (SLC22A4) XP_016865265.1:p.Glu18Lys
NM_003059.3:c.580G>A (SLC22A4) MANE Select NP_003050.2:p.Glu194Lys