Canonical Allele Identifier: CA3403451

Gene: SLC22A4 MIR3936HG

Linked Data

• ClinVar Variation Id: 1669925
• ClinVar RCV Id: RCV002201104
• dbSNP Id: rs11568498
• ExAC: 5:131649415 C / T
• gnomAD v2: 5-131649415-C-T
• gnomAD v3: 5-132313722-C-T
• gnomAD v4: 5-132313722-C-T
• MyVariant Identifiers: chr5:g.131649415C>T (hg19) ; chr5:g.132313722C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313722C>T , CM000667.2:g.132313722C>T	GRCh38
NC_000005.9:g.131649415C>T , CM000667.1:g.131649415C>T	GRCh37
NC_000005.8:g.131677314C>T	NCBI36
NG_012129.1:g.24271C>T
NG_012129.2:g.24271C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.606C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Ile202=
ENST00000200652.3:c.606C>T (SLC22A4)	ENSP00000200652.3:p.Ile202=
ENST00000491257.1:n.410C>T (SLC22A4)
NM_003059.2:c.606C>T (SLC22A4)	NP_003050.2:p.Ile202=
NR_110997.1:n.825-1469G>A (MIR3936HG)
XM_006714675.2:c.78C>T (SLC22A4)	XP_006714738.1:p.Ile26=
XM_011543589.1:c.502C>T (SLC22A4)	XP_011541891.1:p.Arg168Cys
XM_006714675.4:c.78C>T (SLC22A4)	XP_006714738.1:p.Ile26=
XM_011543589.2:c.502C>T (SLC22A4)	XP_011541891.1:p.Arg168Cys
XM_017009776.1:c.78C>T (SLC22A4)	XP_016865265.1:p.Ile26=
NM_003059.3:c.606C>T (SLC22A4) MANE Select	NP_003050.2:p.Ile202=