Canonical Allele Identifier: CA127189157

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs528144935
• gnomAD v2: 5-131649139-T-C
• gnomAD v3: 5-132313446-T-C
• gnomAD v4: 5-132313446-T-C
• MyVariant Identifiers: chr5:g.131649139T>C (hg19) ; chr5:g.132313446T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313446T>C , CM000667.2:g.132313446T>C	GRCh38
NC_000005.9:g.131649139T>C , CM000667.1:g.131649139T>C	GRCh37
NC_000005.8:g.131677038T>C	NCBI36
NG_012129.1:g.23995T>C
NG_012129.2:g.23995T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.498-168T>C (SLC22A4) MANE Select	ENSP00000200652.3:n.498-168T>C
ENST00000200652.3:c.498-168T>C (SLC22A4)	ENSP00000200652.3:n.498-168T>C
ENST00000491257.1:n.302-168T>C (SLC22A4)
NM_003059.2:c.498-168T>C (SLC22A4)	NP_003050.2:n.498-168T>C
NR_110997.1:n.825-1193A>G (MIR3936HG)
XM_006714675.2:c.-31-168T>C (SLC22A4)	XP_006714738.1:n.-31-168T>C
XM_011543589.1:c.394-168T>C (SLC22A4)	XP_011541891.1:n.394-168T>C
XM_006714675.4:c.-31-168T>C (SLC22A4)	XP_006714738.1:n.-31-168T>C
XM_011543589.2:c.394-168T>C (SLC22A4)	XP_011541891.1:n.394-168T>C
XM_017009776.1:c.-31-168T>C (SLC22A4)	XP_016865265.1:n.-31-168T>C
NM_003059.3:c.498-168T>C (SLC22A4) MANE Select	NP_003050.2:n.498-168T>C