Canonical Allele Identifier: CA15402099
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs272869

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132342304A>G , CM000667.2:g.132342304A>G GRCh38
NC_000005.9:g.131677997A>G , CM000667.1:g.131677997A>G GRCh37
NC_000005.8:g.131705896A>G NCBI36
NG_012129.1:g.52853A>G
NG_012129.2:g.52853A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1581-1456A>G (SLC22A4) MANE Select ENSP00000200652.3:n.1581-1456A>G
ENST00000200652.3:c.1581-1456A>G (SLC22A4) ENSP00000200652.3:n.1581-1456A>G
NM_003059.2:c.1581-1456A>G (SLC22A4) NP_003050.2:n.1581-1456A>G
NR_110997.1:n.561-7378T>C (MIR3936HG)
XM_006714675.2:c.1053-1456A>G (SLC22A4) XP_006714738.1:n.1053-1456A>G
XM_011543589.1:c.1305-1456A>G (SLC22A4) XP_011541891.1:n.1305-1456A>G
XM_006714675.4:c.1053-1456A>G (SLC22A4) XP_006714738.1:n.1053-1456A>G
XM_011543589.2:c.1305-1456A>G (SLC22A4) XP_011541891.1:n.1305-1456A>G
XM_017009776.1:c.1053-1456A>G (SLC22A4) XP_016865265.1:n.1053-1456A>G
NM_003059.3:c.1581-1456A>G (SLC22A4) MANE Select NP_003050.2:n.1581-1456A>G