Canonical Allele Identifier: CA1081631876
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI
gnomAD v3:
5:132316836 A / T
gnomAD v4:
chr5-132316836-A-T
Joint Max Group AF 0.00007279 (SAS)
Genomes Max Group AF 0.00007279 (SAS)
dbSNP:
11950562
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132316836A>T , CM000667.2:g.132316836A>T GRCh38
NC_000005.9:g.131652529A>T , CM000667.1:g.131652529A>T GRCh37
NC_000005.8:g.131680428A>T NCBI36
NG_012129.1:g.27385A>T
NG_012129.2:g.27385A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.652+3068A>T (SLC22A4) MANE Select ENSP00000200652.3:n.652+3068A>T
ENST00000200652.3:c.652+3068A>T (SLC22A4) ENSP00000200652.3:n.652+3068A>T
ENST00000491257.1:n.456+3068A>T (SLC22A4)
NM_003059.2:c.652+3068A>T (SLC22A4) NP_003050.2:n.652+3068A>T
NR_110997.1:n.825-4583T>A (MIR3936HG)
XM_006714675.2:c.124+3068A>T (SLC22A4) XP_006714738.1:n.124+3068A>T
XM_011543589.1:c.548+3068A>T (SLC22A4) XP_011541891.1:n.548+3068A>T
XM_006714675.4:c.124+3068A>T (SLC22A4) XP_006714738.1:n.124+3068A>T
XM_011543589.2:c.548+3068A>T (SLC22A4) XP_011541891.1:n.548+3068A>T
XM_017009776.1:c.124+3068A>T (SLC22A4) XP_016865265.1:n.124+3068A>T
NM_003059.3:c.652+3068A>T (SLC22A4) MANE Select NP_003050.2:n.652+3068A>T
Search 100 bp 5'
Search 100 bp 3'