Canonical Allele Identifier: CA360812949

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1434516705
• gnomAD v2: 5-131676290-A-T
• gnomAD v4: 5-132340597-A-T
• MyVariant Identifiers: chr5:g.131676290A>T (hg19) ; chr5:g.132340597A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340597A>T , CM000667.2:g.132340597A>T	GRCh38
NC_000005.9:g.131676290A>T , CM000667.1:g.131676290A>T	GRCh37
NC_000005.8:g.131704189A>T	NCBI36
NG_012129.1:g.51146A>T
NG_012129.2:g.51146A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1477A>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Met493Leu
ENST00000200652.3:c.1477A>T (SLC22A4)	ENSP00000200652.3:p.Met493Leu
NM_003059.2:c.1477A>T (SLC22A4)	NP_003050.2:p.Met493Leu
NR_110997.1:n.561-5671T>A (MIR3936HG)
XM_006714675.2:c.949A>T (SLC22A4)	XP_006714738.1:p.Met317Leu
XM_011543589.1:c.1201A>T (SLC22A4)	XP_011541891.1:p.Met401Leu
XM_006714675.4:c.949A>T (SLC22A4)	XP_006714738.1:p.Met317Leu
XM_011543589.2:c.1201A>T (SLC22A4)	XP_011541891.1:p.Met401Leu
XM_017009776.1:c.949A>T (SLC22A4)	XP_016865265.1:p.Met317Leu
NM_003059.3:c.1477A>T (SLC22A4) MANE Select	NP_003050.2:p.Met493Leu