Canonical Allele Identifier: CA360803903

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649351C>T (hg19) ; chr5:g.132313658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313658C>T , CM000667.2:g.132313658C>T	GRCh38
NC_000005.9:g.131649351C>T , CM000667.1:g.131649351C>T	GRCh37
NC_000005.8:g.131677250C>T	NCBI36
NG_012129.1:g.24207C>T
NG_012129.2:g.24207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.542C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr181Ile
ENST00000200652.3:c.542C>T (SLC22A4)	ENSP00000200652.3:p.Thr181Ile
ENST00000491257.1:n.346C>T (SLC22A4)
NM_003059.2:c.542C>T (SLC22A4)	NP_003050.2:p.Thr181Ile
NR_110997.1:n.825-1405G>A (MIR3936HG)
XM_006714675.2:c.14C>T (SLC22A4)	XP_006714738.1:p.Thr5Ile
XM_011543589.1:c.438C>T (SLC22A4)	XP_011541891.1:p.Asp146=
XM_006714675.4:c.14C>T (SLC22A4)	XP_006714738.1:p.Thr5Ile
XM_011543589.2:c.438C>T (SLC22A4)	XP_011541891.1:p.Asp146=
XM_017009776.1:c.14C>T (SLC22A4)	XP_016865265.1:p.Thr5Ile
NM_003059.3:c.542C>T (SLC22A4) MANE Select	NP_003050.2:p.Thr181Ile