Canonical Allele Identifier: CA2675191146

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132313889-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313889G>C , CM000667.2:g.132313889G>C	GRCh38
NC_000005.9:g.131649582G>C , CM000667.1:g.131649582G>C	GRCh37
NC_000005.8:g.131677481G>C	NCBI36
NG_012129.1:g.24438G>C
NG_012129.2:g.24438G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+121G>C (SLC22A4) MANE Select	ENSP00000200652.3:n.652+121G>C
ENST00000200652.3:c.652+121G>C (SLC22A4)	ENSP00000200652.3:n.652+121G>C
ENST00000491257.1:n.456+121G>C (SLC22A4)
NM_003059.2:c.652+121G>C (SLC22A4)	NP_003050.2:n.652+121G>C
NR_110997.1:n.825-1636C>G (MIR3936HG)
XM_006714675.2:c.124+121G>C (SLC22A4)	XP_006714738.1:n.124+121G>C
XM_011543589.1:c.548+121G>C (SLC22A4)	XP_011541891.1:n.548+121G>C
XM_006714675.4:c.124+121G>C (SLC22A4)	XP_006714738.1:n.124+121G>C
XM_011543589.2:c.548+121G>C (SLC22A4)	XP_011541891.1:n.548+121G>C
XM_017009776.1:c.124+121G>C (SLC22A4)	XP_016865265.1:n.124+121G>C
NM_003059.3:c.652+121G>C (SLC22A4) MANE Select	NP_003050.2:n.652+121G>C