Canonical Allele Identifier: CA2580590918

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132331660A>T , CM000667.2:g.132331660A>T	GRCh38
NC_000005.9:g.131667353A>T , CM000667.1:g.131667353A>T	GRCh37
NC_000005.8:g.131695252A>T	NCBI36
NG_012129.1:g.42209A>T
NG_012129.2:g.42209A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.952-96A>T (SLC22A4) MANE Select	ENSP00000200652.3:n.952-96A>T
ENST00000200652.3:c.952-96A>T (SLC22A4)	ENSP00000200652.3:n.952-96A>T
NM_003059.2:c.952-96A>T (SLC22A4)	NP_003050.2:n.952-96A>T
NR_110997.1:n.824+529T>A (MIR3936HG)
XM_006714675.2:c.424-96A>T (SLC22A4)	XP_006714738.1:n.424-96A>T
XM_011543589.1:c.676-96A>T (SLC22A4)	XP_011541891.1:n.676-96A>T
XM_006714675.4:c.424-96A>T (SLC22A4)	XP_006714738.1:n.424-96A>T
XM_011543589.2:c.676-96A>T (SLC22A4)	XP_011541891.1:n.676-96A>T
XM_017009776.1:c.424-96A>T (SLC22A4)	XP_016865265.1:n.424-96A>T
NM_003059.3:c.952-96A>T (SLC22A4) MANE Select	NP_003050.2:n.952-96A>T