Canonical Allele Identifier: CA127203765

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs112413823
• gnomAD v2: 5-131671330-C-T
• gnomAD v3: 5-132335637-C-T
• gnomAD v4: 5-132335637-C-T
• MyVariant Identifiers: chr5:g.131671330C>T (hg19) ; chr5:g.132335637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132335637C>T , CM000667.2:g.132335637C>T	GRCh38
NC_000005.9:g.131671330C>T , CM000667.1:g.131671330C>T	GRCh37
NC_000005.8:g.131699229C>T	NCBI36
NG_012129.1:g.46186C>T
NG_012129.2:g.46186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1262-181C>T (SLC22A4) MANE Select	ENSP00000200652.3:n.1262-181C>T
ENST00000200652.3:c.1262-181C>T (SLC22A4)	ENSP00000200652.3:n.1262-181C>T
NM_003059.2:c.1262-181C>T (SLC22A4)	NP_003050.2:n.1262-181C>T
NR_110997.1:n.561-711G>A (MIR3936HG)
XM_006714675.2:c.734-181C>T (SLC22A4)	XP_006714738.1:n.734-181C>T
XM_011543589.1:c.986-181C>T (SLC22A4)	XP_011541891.1:n.986-181C>T
XM_006714675.4:c.734-181C>T (SLC22A4)	XP_006714738.1:n.734-181C>T
XM_011543589.2:c.986-181C>T (SLC22A4)	XP_011541891.1:n.986-181C>T
XM_017009776.1:c.734-181C>T (SLC22A4)	XP_016865265.1:n.734-181C>T
NM_003059.3:c.1262-181C>T (SLC22A4) MANE Select	NP_003050.2:n.1262-181C>T