Canonical Allele Identifier: CA348024473

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1558699503
• gnomAD v4: 2-108378495-A-G
• MyVariant Identifiers: chr2:g.108994951A>G (hg19) ; chr2:g.108378495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378495A>G , CM000664.2:g.108378495A>G	GRCh38
NC_000002.11:g.108994951A>G , CM000664.1:g.108994951A>G	GRCh37
NC_000002.10:g.108361383A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.158A>G MANE Select	ENSP00000272452.2:p.Tyr53Cys
ENST00000272452.6:c.158A>G	ENSP00000272452.2:p.Tyr53Cys
ENST00000409309.3:c.158A>G	ENSP00000387225.3:p.Tyr53Cys
ENST00000494122.1:n.585A>G
NM_006588.2:c.158A>G	NP_006579.2:p.Tyr53Cys
XM_005263919.2:c.158A>G	XP_005263976.1:p.Tyr53Cys
NM_001321770.1:c.158A>G	NP_001308699.1:p.Tyr53Cys
NM_006588.3:c.158A>G	NP_006579.2:p.Tyr53Cys
NR_135776.1:n.585A>G
NR_135779.1:n.585A>G
XM_017003807.1:c.-163A>G	XP_016859296.1:n.-163A>G
NM_006588.4:c.158A>G MANE Select	NP_006579.2:p.Tyr53Cys
NM_001321770.2:c.158A>G	NP_001308699.1:p.Tyr53Cys
NR_135776.2:n.542A>G
NR_135779.2:n.542A>G