Canonical Allele Identifier: CA3403457
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

ClinVar Variation Id: 2722859
ClinVar RCV Id: RCV003559114
dbSNP Id: rs143879161
ExAC: 5:131649439 C / G
gnomAD v2: 5-131649439-C-G
gnomAD v3: 5-132313746-C-G
gnomAD v4: 5-132313746-C-G
MyVariant Identifiers: chr5:g.131649439C>G (hg19) chr5:g.132313746C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313746C>G , CM000667.2:g.132313746C>G GRCh38
NC_000005.9:g.131649439C>G , CM000667.1:g.131649439C>G GRCh37
NC_000005.8:g.131677338C>G NCBI36
NG_012129.1:g.24295C>G
NG_012129.2:g.24295C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.630C>G (SLC22A4) MANE Select ENSP00000200652.3:p.Asn210Lys
ENST00000200652.3:c.630C>G (SLC22A4) ENSP00000200652.3:p.Asn210Lys
ENST00000491257.1:n.434C>G (SLC22A4)
NM_003059.2:c.630C>G (SLC22A4) NP_003050.2:p.Asn210Lys
NR_110997.1:n.825-1493G>C (MIR3936HG)
XM_006714675.2:c.102C>G (SLC22A4) XP_006714738.1:p.Asn34Lys
XM_011543589.1:c.526C>G (SLC22A4) XP_011541891.1:p.Leu176Val
XM_006714675.4:c.102C>G (SLC22A4) XP_006714738.1:p.Asn34Lys
XM_011543589.2:c.526C>G (SLC22A4) XP_011541891.1:p.Leu176Val
XM_017009776.1:c.102C>G (SLC22A4) XP_016865265.1:p.Asn34Lys
NM_003059.3:c.630C>G (SLC22A4) MANE Select NP_003050.2:p.Asn210Lys
Search 100 bp 5'
Search 100 bp 3'