Canonical Allele Identifier: CA3403460

Gene: SLC22A4 MIR3936HG

Linked Data

• ClinVar Variation Id: 2994734
• ClinVar RCV Id: RCV003858357
• dbSNP Id: rs376697042
• ExAC: 5:131649448 A / G
• gnomAD v2: 5-131649448-A-G
• gnomAD v3: 5-132313755-A-G
• gnomAD v4: 5-132313755-A-G
• MyVariant Identifiers: chr5:g.131649448A>G (hg19) ; chr5:g.132313755A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313755A>G , CM000667.2:g.132313755A>G	GRCh38
NC_000005.9:g.131649448A>G , CM000667.1:g.131649448A>G	GRCh37
NC_000005.8:g.131677347A>G	NCBI36
NG_012129.1:g.24304A>G
NG_012129.2:g.24304A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.639A>G (SLC22A4) MANE Select	ENSP00000200652.3:p.Val213=
ENST00000200652.3:c.639A>G (SLC22A4)	ENSP00000200652.3:p.Val213=
ENST00000491257.1:n.443A>G (SLC22A4)
NM_003059.2:c.639A>G (SLC22A4)	NP_003050.2:p.Val213=
NR_110997.1:n.825-1502T>C (MIR3936HG)
XM_006714675.2:c.111A>G (SLC22A4)	XP_006714738.1:p.Val37=
XM_011543589.1:c.535A>G (SLC22A4)	XP_011541891.1:p.Ser179Gly
XM_006714675.4:c.111A>G (SLC22A4)	XP_006714738.1:p.Val37=
XM_011543589.2:c.535A>G (SLC22A4)	XP_011541891.1:p.Ser179Gly
XM_017009776.1:c.111A>G (SLC22A4)	XP_016865265.1:p.Val37=
NM_003059.3:c.639A>G (SLC22A4) MANE Select	NP_003050.2:p.Val213=