Canonical Allele Identifier: CA3403469

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs559492142
• ExAC: 5:131649488 T / G
• gnomAD v2: 5-131649488-T-G
• gnomAD v3: 5-132313795-T-G
• gnomAD v4: 5-132313795-T-G
• MyVariant Identifiers: chr5:g.131649488T>G (hg19) ; chr5:g.132313795T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313795T>G , CM000667.2:g.132313795T>G	GRCh38
NC_000005.9:g.131649488T>G , CM000667.1:g.131649488T>G	GRCh37
NC_000005.8:g.131677387T>G	NCBI36
NG_012129.1:g.24344T>G
NG_012129.2:g.24344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+27T>G (SLC22A4) MANE Select	ENSP00000200652.3:n.652+27T>G
ENST00000200652.3:c.652+27T>G (SLC22A4)	ENSP00000200652.3:n.652+27T>G
ENST00000491257.1:n.456+27T>G (SLC22A4)
NM_003059.2:c.652+27T>G (SLC22A4)	NP_003050.2:n.652+27T>G
NR_110997.1:n.825-1542A>C (MIR3936HG)
XM_006714675.2:c.124+27T>G (SLC22A4)	XP_006714738.1:n.124+27T>G
XM_011543589.1:c.548+27T>G (SLC22A4)	XP_011541891.1:n.548+27T>G
XM_006714675.4:c.124+27T>G (SLC22A4)	XP_006714738.1:n.124+27T>G
XM_011543589.2:c.548+27T>G (SLC22A4)	XP_011541891.1:n.548+27T>G
XM_017009776.1:c.124+27T>G (SLC22A4)	XP_016865265.1:n.124+27T>G
NM_003059.3:c.652+27T>G (SLC22A4) MANE Select	NP_003050.2:n.652+27T>G