Canonical Allele Identifier: CA446335143

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs272879
• MyVariant Identifiers: chr5:g.131670546C>T (hg19) ; chr5:g.132334853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132334853C>T , CM000667.2:g.132334853C>T	GRCh38
NC_000005.9:g.131670546C>T , CM000667.1:g.131670546C>T	GRCh37
NC_000005.8:g.131698445C>T	NCBI36
NG_012129.1:g.45402C>T
NG_012129.2:g.45402C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1182C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr394=
ENST00000200652.3:c.1182C>T (SLC22A4)	ENSP00000200652.3:p.Thr394=
NM_003059.2:c.1182C>T (SLC22A4)	NP_003050.2:p.Thr394=
NR_110997.1:n.634G>A (MIR3936HG)
XM_006714675.2:c.654C>T (SLC22A4)	XP_006714738.1:p.Thr218=
XM_011543589.1:c.906C>T (SLC22A4)	XP_011541891.1:p.Thr302=
XM_006714675.4:c.654C>T (SLC22A4)	XP_006714738.1:p.Thr218=
XM_011543589.2:c.906C>T (SLC22A4)	XP_011541891.1:p.Thr302=
XM_017009776.1:c.654C>T (SLC22A4)	XP_016865265.1:p.Thr218=
NM_003059.3:c.1182C>T (SLC22A4) MANE Select	NP_003050.2:p.Thr394=