Canonical Allele Identifier: CA3403623
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.132335767G>A
GRCh37 chr5:g.131671460G>A
gnomAD v2:
5:131671460 G / A
gnomAD v3:
5:132335767 G / A
gnomAD v4:
chr5-132335767-G-A
Joint Max Group AF 0.02276436 (NFE)
Genomes Max Group AF 0.02072009 (NFE)
Exomes Max Group AF 0.02415386 (AMR)
dbSNP:
11568506
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132335767G>A , CM000667.2:g.132335767G>A GRCh38
NC_000005.9:g.131671460G>A , CM000667.1:g.131671460G>A GRCh37
NC_000005.8:g.131699359G>A NCBI36
NG_012129.1:g.46316G>A
NG_012129.2:g.46316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1262-51G>A (SLC22A4) MANE Select ENSP00000200652.3:n.1262-51G>A
ENST00000200652.3:c.1262-51G>A (SLC22A4) ENSP00000200652.3:n.1262-51G>A
NM_003059.2:c.1262-51G>A (SLC22A4) NP_003050.2:n.1262-51G>A
NR_110997.1:n.561-841C>T (MIR3936HG)
XM_006714675.2:c.734-51G>A (SLC22A4) XP_006714738.1:n.734-51G>A
XM_011543589.1:c.986-51G>A (SLC22A4) XP_011541891.1:n.986-51G>A
XM_006714675.4:c.734-51G>A (SLC22A4) XP_006714738.1:n.734-51G>A
XM_011543589.2:c.986-51G>A (SLC22A4) XP_011541891.1:n.986-51G>A
XM_017009776.1:c.734-51G>A (SLC22A4) XP_016865265.1:n.734-51G>A
NM_003059.3:c.1262-51G>A (SLC22A4) MANE Select NP_003050.2:n.1262-51G>A
Search 100 bp 5'
Search 100 bp 3'