Canonical Allele Identifier: CA1583118580

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1750257363
• gnomAD v4: 5-132313843-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313843C>T , CM000667.2:g.132313843C>T	GRCh38
NC_000005.9:g.131649536C>T , CM000667.1:g.131649536C>T	GRCh37
NC_000005.8:g.131677435C>T	NCBI36
NG_012129.1:g.24392C>T
NG_012129.2:g.24392C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+75C>T (SLC22A4) MANE Select	ENSP00000200652.3:n.652+75C>T
ENST00000200652.3:c.652+75C>T (SLC22A4)	ENSP00000200652.3:n.652+75C>T
ENST00000491257.1:n.456+75C>T (SLC22A4)
NM_003059.2:c.652+75C>T (SLC22A4)	NP_003050.2:n.652+75C>T
NR_110997.1:n.825-1590G>A (MIR3936HG)
XM_006714675.2:c.124+75C>T (SLC22A4)	XP_006714738.1:n.124+75C>T
XM_011543589.1:c.548+75C>T (SLC22A4)	XP_011541891.1:n.548+75C>T
XM_006714675.4:c.124+75C>T (SLC22A4)	XP_006714738.1:n.124+75C>T
XM_011543589.2:c.548+75C>T (SLC22A4)	XP_011541891.1:n.548+75C>T
XM_017009776.1:c.124+75C>T (SLC22A4)	XP_016865265.1:n.124+75C>T
NM_003059.3:c.652+75C>T (SLC22A4) MANE Select	NP_003050.2:n.652+75C>T