Canonical Allele Identifier: CA348019818

Gene: SULT1C3

Linked Data

• MyVariant Identifiers: chr2:g.108875204T>A (hg19) ; chr2:g.108258748T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108258748T>A , CM000664.2:g.108258748T>A	GRCh38
NC_000002.11:g.108875204T>A , CM000664.1:g.108875204T>A	GRCh37
NC_000002.10:g.108241636T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681802.2:c.541T>A MANE Select	ENSP00000505748.1:p.Trp181Arg
ENST00000329106.3:c.541T>A	ENSP00000333310.2:p.Trp181Arg
ENST00000681802.1:c.541T>A	ENSP00000505748.1:p.Trp181Arg
ENST00000329106.2:c.541T>A	ENSP00000333310.2:p.Trp181Arg
NM_001008743.1:c.541T>A	NP_001008743.1:p.Trp181Arg
XM_011511209.1:c.541T>A	XP_011509511.1:p.Trp181Arg
XM_011511210.1:c.541T>A	XP_011509512.1:p.Trp181Arg
XM_011511211.1:c.541T>A	XP_011509513.1:p.Trp181Arg
XM_011511212.1:c.541T>A	XP_011509514.1:p.Trp181Arg
NM_001008743.2:c.541T>A	NP_001008743.1:p.Trp181Arg
NM_001320878.1:c.541T>A	NP_001307807.1:p.Trp181Arg
XM_017004153.1:c.676T>A	XP_016859642.1:p.Trp226Arg
XM_017004154.1:c.676T>A	XP_016859643.1:p.Trp226Arg
XM_017004155.1:c.676T>A	XP_016859644.1:p.Trp226Arg
NM_001008743.3:c.541T>A	NP_001008743.1:p.Trp181Arg
NM_001320878.2:c.541T>A MANE Select	NP_001307807.1:p.Trp181Arg