Canonical Allele Identifier: CA2660570926

Gene: SULT1C3

Linked Data

• gnomAD v4: 2-108258673-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108258673A>G , CM000664.2:g.108258673A>G	GRCh38
NC_000002.11:g.108875129A>G , CM000664.1:g.108875129A>G	GRCh37
NC_000002.10:g.108241561A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681802.2:c.527-61A>G MANE Select	ENSP00000505748.1:n.527-61A>G
ENST00000329106.3:c.527-61A>G	ENSP00000333310.2:n.527-61A>G
ENST00000681802.1:c.527-61A>G	ENSP00000505748.1:n.527-61A>G
ENST00000329106.2:c.527-61A>G	ENSP00000333310.2:n.527-61A>G
NM_001008743.1:c.527-61A>G	NP_001008743.1:n.527-61A>G
XM_011511209.1:c.527-61A>G	XP_011509511.1:n.527-61A>G
XM_011511210.1:c.527-61A>G	XP_011509512.1:n.527-61A>G
XM_011511211.1:c.527-61A>G	XP_011509513.1:n.527-61A>G
XM_011511212.1:c.527-61A>G	XP_011509514.1:n.527-61A>G
NM_001008743.2:c.527-61A>G	NP_001008743.1:n.527-61A>G
NM_001320878.1:c.527-61A>G	NP_001307807.1:n.527-61A>G
XM_017004153.1:c.662-61A>G	XP_016859642.1:n.662-61A>G
XM_017004154.1:c.662-61A>G	XP_016859643.1:n.662-61A>G
XM_017004155.1:c.662-61A>G	XP_016859644.1:n.662-61A>G
NM_001008743.3:c.527-61A>G	NP_001008743.1:n.527-61A>G
NM_001320878.2:c.527-61A>G MANE Select	NP_001307807.1:n.527-61A>G