Canonical Allele Identifier: CA348024427

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1466118688
• gnomAD v2: 2-108994935-C-G
• MyVariant Identifiers: chr2:g.108994935C>G (hg19) ; chr2:g.108378479C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378479C>G , CM000664.2:g.108378479C>G	GRCh38
NC_000002.11:g.108994935C>G , CM000664.1:g.108994935C>G	GRCh37
NC_000002.10:g.108361367C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.142C>G MANE Select	ENSP00000272452.2:p.Leu48Val
ENST00000272452.6:c.142C>G	ENSP00000272452.2:p.Leu48Val
ENST00000409309.3:c.142C>G	ENSP00000387225.3:p.Leu48Val
ENST00000494122.1:n.569C>G
NM_006588.2:c.142C>G	NP_006579.2:p.Leu48Val
XM_005263919.2:c.142C>G	XP_005263976.1:p.Leu48Val
NM_001321770.1:c.142C>G	NP_001308699.1:p.Leu48Val
NM_006588.3:c.142C>G	NP_006579.2:p.Leu48Val
NR_135776.1:n.569C>G
NR_135779.1:n.569C>G
XM_017003807.1:c.-179C>G	XP_016859296.1:n.-179C>G
NM_006588.4:c.142C>G MANE Select	NP_006579.2:p.Leu48Val
NM_001321770.2:c.142C>G	NP_001308699.1:p.Leu48Val
NR_135776.2:n.526C>G
NR_135779.2:n.526C>G