Canonical Allele Identifier: CA1819919
Gene: SULT1C4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2380463
ClinVar RCV Id: RCV004218958
dbSNP Id: rs374459677

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378356G>C , CM000664.2:g.108378356G>C GRCh38
NC_000002.11:g.108994812G>C , CM000664.1:g.108994812G>C GRCh37
NC_000002.10:g.108361244G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.19G>C MANE Select ENSP00000272452.2:p.Glu7Gln
ENST00000272452.6:c.19G>C ENSP00000272452.2:p.Glu7Gln
ENST00000409309.3:c.19G>C ENSP00000387225.3:p.Glu7Gln
ENST00000494122.1:n.446G>C
NM_006588.2:c.19G>C NP_006579.2:p.Glu7Gln
XM_005263919.2:c.19G>C XP_005263976.1:p.Glu7Gln
NM_001321770.1:c.19G>C NP_001308699.1:p.Glu7Gln
NM_006588.3:c.19G>C NP_006579.2:p.Glu7Gln
NR_135776.1:n.446G>C
NR_135779.1:n.446G>C
NM_006588.4:c.19G>C MANE Select NP_006579.2:p.Glu7Gln
NM_001321770.2:c.19G>C NP_001308699.1:p.Glu7Gln
NR_135776.2:n.403G>C
NR_135779.2:n.403G>C