Canonical Allele Identifier: CA348024310

Gene: SULT1C4

Linked Data

• gnomAD v4: 2-108378444-A-G
• MyVariant Identifiers: chr2:g.108994900A>G (hg19) ; chr2:g.108378444A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378444A>G , CM000664.2:g.108378444A>G	GRCh38
NC_000002.11:g.108994900A>G , CM000664.1:g.108994900A>G	GRCh37
NC_000002.10:g.108361332A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.107A>G MANE Select	ENSP00000272452.2:p.Asp36Gly
ENST00000272452.6:c.107A>G	ENSP00000272452.2:p.Asp36Gly
ENST00000409309.3:c.107A>G	ENSP00000387225.3:p.Asp36Gly
ENST00000494122.1:n.534A>G
NM_006588.2:c.107A>G	NP_006579.2:p.Asp36Gly
XM_005263919.2:c.107A>G	XP_005263976.1:p.Asp36Gly
NM_001321770.1:c.107A>G	NP_001308699.1:p.Asp36Gly
NM_006588.3:c.107A>G	NP_006579.2:p.Asp36Gly
NR_135776.1:n.534A>G
NR_135779.1:n.534A>G
XM_017003807.1:c.-214A>G	XP_016859296.1:n.-214A>G
NM_006588.4:c.107A>G MANE Select	NP_006579.2:p.Asp36Gly
NM_001321770.2:c.107A>G	NP_001308699.1:p.Asp36Gly
NR_135776.2:n.491A>G
NR_135779.2:n.491A>G