Canonical Allele Identifier: CA127188285
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs11568510
MyVariant Identifiers: chr5:g.131647954A>G (hg19) chr5:g.132312261A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132312261A>G , CM000667.2:g.132312261A>G GRCh38
NC_000005.9:g.131647954A>G , CM000667.1:g.131647954A>G GRCh37
NC_000005.8:g.131675853A>G NCBI36
NG_012129.1:g.22810A>G
NG_012129.2:g.22810A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.494A>G (SLC22A4) MANE Select ENSP00000200652.3:p.Asp165Gly
ENST00000200652.3:c.494A>G (SLC22A4) ENSP00000200652.3:p.Asp165Gly
ENST00000491257.1:n.298A>G (SLC22A4)
NM_003059.2:c.494A>G (SLC22A4) NP_003050.2:p.Asp165Gly
NR_110997.1:n.825-8T>C (MIR3936HG)
XM_006714675.2:c.-31-1353A>G (SLC22A4) XP_006714738.1:n.-31-1353A>G
XM_011543589.1:c.394-1353A>G (SLC22A4) XP_011541891.1:n.394-1353A>G
XM_006714675.4:c.-31-1353A>G (SLC22A4) XP_006714738.1:n.-31-1353A>G
XM_011543589.2:c.394-1353A>G (SLC22A4) XP_011541891.1:n.394-1353A>G
XM_017009776.1:c.-35A>G (SLC22A4) XP_016865265.1:n.-35A>G
NM_003059.3:c.494A>G (SLC22A4) MANE Select NP_003050.2:p.Asp165Gly
Search 100 bp 5'
Search 100 bp 3'