Canonical Allele Identifier: CA348024066

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1202365786
• gnomAD v2: 2-108994839-C-T
• gnomAD v3: 2-108378383-C-T
• gnomAD v4: 2-108378383-C-T
• MyVariant Identifiers: chr2:g.108994839C>T (hg19) ; chr2:g.108378383C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378383C>T , CM000664.2:g.108378383C>T	GRCh38
NC_000002.11:g.108994839C>T , CM000664.1:g.108994839C>T	GRCh37
NC_000002.10:g.108361271C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.46C>T MANE Select	ENSP00000272452.2:p.Arg16Cys
ENST00000272452.6:c.46C>T	ENSP00000272452.2:p.Arg16Cys
ENST00000409309.3:c.46C>T	ENSP00000387225.3:p.Arg16Cys
ENST00000494122.1:n.473C>T
NM_006588.2:c.46C>T	NP_006579.2:p.Arg16Cys
XM_005263919.2:c.46C>T	XP_005263976.1:p.Arg16Cys
NM_001321770.1:c.46C>T	NP_001308699.1:p.Arg16Cys
NM_006588.3:c.46C>T	NP_006579.2:p.Arg16Cys
NR_135776.1:n.473C>T
NR_135779.1:n.473C>T
NM_006588.4:c.46C>T MANE Select	NP_006579.2:p.Arg16Cys
NM_001321770.2:c.46C>T	NP_001308699.1:p.Arg16Cys
NR_135776.2:n.430C>T
NR_135779.2:n.430C>T