Canonical Allele Identifier: CA2577062348

Gene: SULT1C3

Linked Data

• dbSNP Id: rs2104392306

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108258670T>C , CM000664.2:g.108258670T>C	GRCh38
NC_000002.11:g.108875126T>C , CM000664.1:g.108875126T>C	GRCh37
NC_000002.10:g.108241558T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681802.2:c.527-64T>C MANE Select	ENSP00000505748.1:n.527-64T>C
ENST00000329106.3:c.527-64T>C	ENSP00000333310.2:n.527-64T>C
ENST00000681802.1:c.527-64T>C	ENSP00000505748.1:n.527-64T>C
ENST00000329106.2:c.527-64T>C	ENSP00000333310.2:n.527-64T>C
NM_001008743.1:c.527-64T>C	NP_001008743.1:n.527-64T>C
XM_011511209.1:c.527-64T>C	XP_011509511.1:n.527-64T>C
XM_011511210.1:c.527-64T>C	XP_011509512.1:n.527-64T>C
XM_011511211.1:c.527-64T>C	XP_011509513.1:n.527-64T>C
XM_011511212.1:c.527-64T>C	XP_011509514.1:n.527-64T>C
NM_001008743.2:c.527-64T>C	NP_001008743.1:n.527-64T>C
NM_001320878.1:c.527-64T>C	NP_001307807.1:n.527-64T>C
XM_017004153.1:c.662-64T>C	XP_016859642.1:n.662-64T>C
XM_017004154.1:c.662-64T>C	XP_016859643.1:n.662-64T>C
XM_017004155.1:c.662-64T>C	XP_016859644.1:n.662-64T>C
NM_001008743.3:c.527-64T>C	NP_001008743.1:n.527-64T>C
NM_001320878.2:c.527-64T>C MANE Select	NP_001307807.1:n.527-64T>C