Canonical Allele Identifier: CA446339828
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.131676259T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340566T>A , CM000667.2:g.132340566T>A GRCh38
NC_000005.9:g.131676259T>A , CM000667.1:g.131676259T>A GRCh37
NC_000005.8:g.131704158T>A NCBI36
NG_012129.1:g.51115T>A
NG_012129.2:g.51115T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1446T>A (SLC22A4) MANE Select ENSP00000200652.3:p.Gly482=
ENST00000200652.3:c.1446T>A (SLC22A4) ENSP00000200652.3:p.Gly482=
NM_003059.2:c.1446T>A (SLC22A4) NP_003050.2:p.Gly482=
NR_110997.1:n.561-5640A>T (MIR3936HG)
XM_006714675.2:c.918T>A (SLC22A4) XP_006714738.1:p.Gly306=
XM_011543589.1:c.1170T>A (SLC22A4) XP_011541891.1:p.Gly390=
XM_006714675.4:c.918T>A (SLC22A4) XP_006714738.1:p.Gly306=
XM_011543589.2:c.1170T>A (SLC22A4) XP_011541891.1:p.Gly390=
XM_017009776.1:c.918T>A (SLC22A4) XP_016865265.1:p.Gly306=
NM_003059.3:c.1446T>A (SLC22A4) MANE Select NP_003050.2:p.Gly482=