Canonical Allele Identifier: CA348019834

Gene: SULT1C3

Linked Data

• MyVariant Identifiers: chr2:g.108875206G>C (hg19) ; chr2:g.108258750G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108258750G>C , CM000664.2:g.108258750G>C	GRCh38
NC_000002.11:g.108875206G>C , CM000664.1:g.108875206G>C	GRCh37
NC_000002.10:g.108241638G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681802.2:c.543G>C MANE Select	ENSP00000505748.1:p.Trp181Cys
ENST00000329106.3:c.543G>C	ENSP00000333310.2:p.Trp181Cys
ENST00000681802.1:c.543G>C	ENSP00000505748.1:p.Trp181Cys
ENST00000329106.2:c.543G>C	ENSP00000333310.2:p.Trp181Cys
NM_001008743.1:c.543G>C	NP_001008743.1:p.Trp181Cys
XM_011511209.1:c.543G>C	XP_011509511.1:p.Trp181Cys
XM_011511210.1:c.543G>C	XP_011509512.1:p.Trp181Cys
XM_011511211.1:c.543G>C	XP_011509513.1:p.Trp181Cys
XM_011511212.1:c.543G>C	XP_011509514.1:p.Trp181Cys
NM_001008743.2:c.543G>C	NP_001008743.1:p.Trp181Cys
NM_001320878.1:c.543G>C	NP_001307807.1:p.Trp181Cys
XM_017004153.1:c.678G>C	XP_016859642.1:p.Trp226Cys
XM_017004154.1:c.678G>C	XP_016859643.1:p.Trp226Cys
XM_017004155.1:c.678G>C	XP_016859644.1:p.Trp226Cys
NM_001008743.3:c.543G>C	NP_001008743.1:p.Trp181Cys
NM_001320878.2:c.543G>C MANE Select	NP_001307807.1:p.Trp181Cys