Canonical Allele Identifier: CA360813138

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131676319C>G (hg19) ; chr5:g.132340626C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340626C>G , CM000667.2:g.132340626C>G	GRCh38
NC_000005.9:g.131676319C>G , CM000667.1:g.131676319C>G	GRCh37
NC_000005.8:g.131704218C>G	NCBI36
NG_012129.1:g.51175C>G
NG_012129.2:g.51175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1506C>G (SLC22A4) MANE Select	ENSP00000200652.3:p.Ile502Met
ENST00000200652.3:c.1506C>G (SLC22A4)	ENSP00000200652.3:p.Ile502Met
NM_003059.2:c.1506C>G (SLC22A4)	NP_003050.2:p.Ile502Met
NR_110997.1:n.561-5700G>C (MIR3936HG)
XM_006714675.2:c.978C>G (SLC22A4)	XP_006714738.1:p.Ile326Met
XM_011543589.1:c.1230C>G (SLC22A4)	XP_011541891.1:p.Ile410Met
XM_006714675.4:c.978C>G (SLC22A4)	XP_006714738.1:p.Ile326Met
XM_011543589.2:c.1230C>G (SLC22A4)	XP_011541891.1:p.Ile410Met
XM_017009776.1:c.978C>G (SLC22A4)	XP_016865265.1:p.Ile326Met
NM_003059.3:c.1506C>G (SLC22A4) MANE Select	NP_003050.2:p.Ile502Met