Canonical Allele Identifier: CA3403695
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs367641793

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340554G>C , CM000667.2:g.132340554G>C GRCh38
NC_000005.9:g.131676247G>C , CM000667.1:g.131676247G>C GRCh37
NC_000005.8:g.131704146G>C NCBI36
NG_012129.1:g.51103G>C
NG_012129.2:g.51103G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1445-11G>C (SLC22A4) MANE Select ENSP00000200652.3:n.1445-11G>C
ENST00000200652.3:c.1445-11G>C (SLC22A4) ENSP00000200652.3:n.1445-11G>C
NM_003059.2:c.1445-11G>C (SLC22A4) NP_003050.2:n.1445-11G>C
NR_110997.1:n.561-5628C>G (MIR3936HG)
XM_006714675.2:c.917-11G>C (SLC22A4) XP_006714738.1:n.917-11G>C
XM_011543589.1:c.1169-11G>C (SLC22A4) XP_011541891.1:n.1169-11G>C
XM_006714675.4:c.917-11G>C (SLC22A4) XP_006714738.1:n.917-11G>C
XM_011543589.2:c.1169-11G>C (SLC22A4) XP_011541891.1:n.1169-11G>C
XM_017009776.1:c.917-11G>C (SLC22A4) XP_016865265.1:n.917-11G>C
NM_003059.3:c.1445-11G>C (SLC22A4) MANE Select NP_003050.2:n.1445-11G>C