Canonical Allele Identifier: CA53420331

Gene: SULT1C4

Linked Data

• dbSNP Id: rs958887553
• gnomAD v2: 2-108994753-A-G
• gnomAD v3: 2-108378297-A-G
• gnomAD v4: 2-108378297-A-G
• MyVariant Identifiers: chr2:g.108994753A>G (hg19) ; chr2:g.108378297A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378297A>G , CM000664.2:g.108378297A>G	GRCh38
NC_000002.11:g.108994753A>G , CM000664.1:g.108994753A>G	GRCh37
NC_000002.10:g.108361185A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-41A>G MANE Select	ENSP00000272452.2:n.-41A>G
ENST00000272452.6:c.-41A>G	ENSP00000272452.2:n.-41A>G
ENST00000409309.3:c.-41A>G	ENSP00000387225.3:n.-41A>G
ENST00000494122.1:n.387A>G
NM_006588.2:c.-41A>G	NP_006579.2:n.-41A>G
XM_005263919.2:c.-41A>G	XP_005263976.1:n.-41A>G
NM_001321770.1:c.-41A>G	NP_001308699.1:n.-41A>G
NM_006588.3:c.-41A>G	NP_006579.2:n.-41A>G
NR_135776.1:n.387A>G
NR_135779.1:n.387A>G
NM_006588.4:c.-41A>G MANE Select	NP_006579.2:n.-41A>G
NM_001321770.2:c.-41A>G	NP_001308699.1:n.-41A>G
NR_135776.2:n.344A>G
NR_135779.2:n.344A>G