Canonical Allele Identifier: CA360804073
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313733G>T , CM000667.2:g.132313733G>T GRCh38
NC_000005.9:g.131649426G>T , CM000667.1:g.131649426G>T GRCh37
NC_000005.8:g.131677325G>T NCBI36
NG_012129.1:g.24282G>T
NG_012129.2:g.24282G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.617G>T (SLC22A4) MANE Select ENSP00000200652.3:p.Gly206Val
ENST00000200652.3:c.617G>T (SLC22A4) ENSP00000200652.3:p.Gly206Val
ENST00000491257.1:n.421G>T (SLC22A4)
NM_003059.2:c.617G>T (SLC22A4) NP_003050.2:p.Gly206Val
NR_110997.1:n.825-1480C>A (MIR3936HG)
XM_006714675.2:c.89G>T (SLC22A4) XP_006714738.1:p.Gly30Val
XM_011543589.1:c.513G>T (SLC22A4) XP_011541891.1:p.Gly171=
XM_006714675.4:c.89G>T (SLC22A4) XP_006714738.1:p.Gly30Val
XM_011543589.2:c.513G>T (SLC22A4) XP_011541891.1:p.Gly171=
XM_017009776.1:c.89G>T (SLC22A4) XP_016865265.1:p.Gly30Val
NM_003059.3:c.617G>T (SLC22A4) MANE Select NP_003050.2:p.Gly206Val