Canonical Allele Identifier: CA348024389

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1678303156
• gnomAD v4: 2-108378462-A-T
• MyVariant Identifiers: chr2:g.108994918A>T (hg19) ; chr2:g.108378462A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378462A>T , CM000664.2:g.108378462A>T	GRCh38
NC_000002.11:g.108994918A>T , CM000664.1:g.108994918A>T	GRCh37
NC_000002.10:g.108361350A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.125A>T MANE Select	ENSP00000272452.2:p.Gln42Leu
ENST00000272452.6:c.125A>T	ENSP00000272452.2:p.Gln42Leu
ENST00000409309.3:c.125A>T	ENSP00000387225.3:p.Gln42Leu
ENST00000494122.1:n.552A>T
NM_006588.2:c.125A>T	NP_006579.2:p.Gln42Leu
XM_005263919.2:c.125A>T	XP_005263976.1:p.Gln42Leu
NM_001321770.1:c.125A>T	NP_001308699.1:p.Gln42Leu
NM_006588.3:c.125A>T	NP_006579.2:p.Gln42Leu
NR_135776.1:n.552A>T
NR_135779.1:n.552A>T
XM_017003807.1:c.-196A>T	XP_016859296.1:n.-196A>T
NM_006588.4:c.125A>T MANE Select	NP_006579.2:p.Gln42Leu
NM_001321770.2:c.125A>T	NP_001308699.1:p.Gln42Leu
NR_135776.2:n.509A>T
NR_135779.2:n.509A>T