Canonical Allele Identifier: CA360813189

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1310924815
• gnomAD v3: 5-132340634-T-C
• gnomAD v4: 5-132340634-T-C
• MyVariant Identifiers: chr5:g.131676327T>C (hg19) ; chr5:g.132340634T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340634T>C , CM000667.2:g.132340634T>C	GRCh38
NC_000005.9:g.131676327T>C , CM000667.1:g.131676327T>C	GRCh37
NC_000005.8:g.131704226T>C	NCBI36
NG_012129.1:g.51183T>C
NG_012129.2:g.51183T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1514T>C (SLC22A4) MANE Select	ENSP00000200652.3:p.Leu505Pro
ENST00000200652.3:c.1514T>C (SLC22A4)	ENSP00000200652.3:p.Leu505Pro
NM_003059.2:c.1514T>C (SLC22A4)	NP_003050.2:p.Leu505Pro
NR_110997.1:n.561-5708A>G (MIR3936HG)
XM_006714675.2:c.986T>C (SLC22A4)	XP_006714738.1:p.Leu329Pro
XM_011543589.1:c.1238T>C (SLC22A4)	XP_011541891.1:p.Leu413Pro
XM_006714675.4:c.986T>C (SLC22A4)	XP_006714738.1:p.Leu329Pro
XM_011543589.2:c.1238T>C (SLC22A4)	XP_011541891.1:p.Leu413Pro
XM_017009776.1:c.986T>C (SLC22A4)	XP_016865265.1:p.Leu329Pro
NM_003059.3:c.1514T>C (SLC22A4) MANE Select	NP_003050.2:p.Leu505Pro