Canonical Allele Identifier: CA360803953

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649374T>G (hg19) ; chr5:g.132313681T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313681T>G , CM000667.2:g.132313681T>G	GRCh38
NC_000005.9:g.131649374T>G , CM000667.1:g.131649374T>G	GRCh37
NC_000005.8:g.131677273T>G	NCBI36
NG_012129.1:g.24230T>G
NG_012129.2:g.24230T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.565T>G (SLC22A4) MANE Select	ENSP00000200652.3:p.Phe189Val
ENST00000200652.3:c.565T>G (SLC22A4)	ENSP00000200652.3:p.Phe189Val
ENST00000491257.1:n.369T>G (SLC22A4)
NM_003059.2:c.565T>G (SLC22A4)	NP_003050.2:p.Phe189Val
NR_110997.1:n.825-1428A>C (MIR3936HG)
XM_006714675.2:c.37T>G (SLC22A4)	XP_006714738.1:p.Phe13Val
XM_011543589.1:c.461T>G (SLC22A4)	XP_011541891.1:p.Phe154Cys
XM_006714675.4:c.37T>G (SLC22A4)	XP_006714738.1:p.Phe13Val
XM_011543589.2:c.461T>G (SLC22A4)	XP_011541891.1:p.Phe154Cys
XM_017009776.1:c.37T>G (SLC22A4)	XP_016865265.1:p.Phe13Val
NM_003059.3:c.565T>G (SLC22A4) MANE Select	NP_003050.2:p.Phe189Val