Canonical Allele Identifier: CA360812713
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340563A>T , CM000667.2:g.132340563A>T GRCh38
NC_000005.9:g.131676256A>T , CM000667.1:g.131676256A>T GRCh37
NC_000005.8:g.131704155A>T NCBI36
NG_012129.1:g.51112A>T
NG_012129.2:g.51112A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1445-2A>T (SLC22A4) MANE Select ENSP00000200652.3:n.1445-2A>T
ENST00000200652.3:c.1445-2A>T (SLC22A4) ENSP00000200652.3:n.1445-2A>T
NM_003059.2:c.1445-2A>T (SLC22A4) NP_003050.2:n.1445-2A>T
NR_110997.1:n.561-5637T>A (MIR3936HG)
XM_006714675.2:c.917-2A>T (SLC22A4) XP_006714738.1:n.917-2A>T
XM_011543589.1:c.1169-2A>T (SLC22A4) XP_011541891.1:n.1169-2A>T
XM_006714675.4:c.917-2A>T (SLC22A4) XP_006714738.1:n.917-2A>T
XM_011543589.2:c.1169-2A>T (SLC22A4) XP_011541891.1:n.1169-2A>T
XM_017009776.1:c.917-2A>T (SLC22A4) XP_016865265.1:n.917-2A>T
NM_003059.3:c.1445-2A>T (SLC22A4) MANE Select NP_003050.2:n.1445-2A>T