Canonical Allele Identifier: CA803998007

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1396014888
• gnomAD v3: 5-132313859-C-T
• gnomAD v4: 5-132313859-C-T
• MyVariant Identifiers: chr5:g.131649552C>T (hg19) ; chr5:g.132313859C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313859C>T , CM000667.2:g.132313859C>T	GRCh38
NC_000005.9:g.131649552C>T , CM000667.1:g.131649552C>T	GRCh37
NC_000005.8:g.131677451C>T	NCBI36
NG_012129.1:g.24408C>T
NG_012129.2:g.24408C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+91C>T (SLC22A4) MANE Select	ENSP00000200652.3:n.652+91C>T
ENST00000200652.3:c.652+91C>T (SLC22A4)	ENSP00000200652.3:n.652+91C>T
ENST00000491257.1:n.456+91C>T (SLC22A4)
NM_003059.2:c.652+91C>T (SLC22A4)	NP_003050.2:n.652+91C>T
NR_110997.1:n.825-1606G>A (MIR3936HG)
XM_006714675.2:c.124+91C>T (SLC22A4)	XP_006714738.1:n.124+91C>T
XM_011543589.1:c.548+91C>T (SLC22A4)	XP_011541891.1:n.548+91C>T
XM_006714675.4:c.124+91C>T (SLC22A4)	XP_006714738.1:n.124+91C>T
XM_011543589.2:c.548+91C>T (SLC22A4)	XP_011541891.1:n.548+91C>T
XM_017009776.1:c.124+91C>T (SLC22A4)	XP_016865265.1:n.124+91C>T
NM_003059.3:c.652+91C>T (SLC22A4) MANE Select	NP_003050.2:n.652+91C>T