Canonical Allele Identifier: CA360803866

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649335A>G (hg19) ; chr5:g.132313642A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313642A>G , CM000667.2:g.132313642A>G	GRCh38
NC_000005.9:g.131649335A>G , CM000667.1:g.131649335A>G	GRCh37
NC_000005.8:g.131677234A>G	NCBI36
NG_012129.1:g.24191A>G
NG_012129.2:g.24191A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.526A>G (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr176Ala
ENST00000200652.3:c.526A>G (SLC22A4)	ENSP00000200652.3:p.Thr176Ala
ENST00000491257.1:n.330A>G (SLC22A4)
NM_003059.2:c.526A>G (SLC22A4)	NP_003050.2:p.Thr176Ala
NR_110997.1:n.825-1389T>C (MIR3936HG)
XM_006714675.2:c.-3A>G (SLC22A4)	XP_006714738.1:n.-3A>G
XM_011543589.1:c.422A>G (SLC22A4)	XP_011541891.1:p.Asn141Ser
XM_006714675.4:c.-3A>G (SLC22A4)	XP_006714738.1:n.-3A>G
XM_011543589.2:c.422A>G (SLC22A4)	XP_011541891.1:p.Asn141Ser
XM_017009776.1:c.-3A>G (SLC22A4)	XP_016865265.1:n.-3A>G
NM_003059.3:c.526A>G (SLC22A4) MANE Select	NP_003050.2:p.Thr176Ala