Canonical Allele Identifier: CA427904938

Gene: SULT1C4

Linked Data

• dbSNP Id: rs763755892
• gnomAD v4: 2-108378499-T-A
• MyVariant Identifiers: chr2:g.108994955T>A (hg19) ; chr2:g.108378499T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378499T>A , CM000664.2:g.108378499T>A	GRCh38
NC_000002.11:g.108994955T>A , CM000664.1:g.108994955T>A	GRCh37
NC_000002.10:g.108361387T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.162T>A MANE Select	ENSP00000272452.2:p.Pro54=
ENST00000272452.6:c.162T>A	ENSP00000272452.2:p.Pro54=
ENST00000409309.3:c.162T>A	ENSP00000387225.3:p.Pro54=
ENST00000494122.1:n.589T>A
NM_006588.2:c.162T>A	NP_006579.2:p.Pro54=
XM_005263919.2:c.162T>A	XP_005263976.1:p.Pro54=
NM_001321770.1:c.162T>A	NP_001308699.1:p.Pro54=
NM_006588.3:c.162T>A	NP_006579.2:p.Pro54=
NR_135776.1:n.589T>A
NR_135779.1:n.589T>A
XM_017003807.1:c.-159T>A	XP_016859296.1:n.-159T>A
NM_006588.4:c.162T>A MANE Select	NP_006579.2:p.Pro54=
NM_001321770.2:c.162T>A	NP_001308699.1:p.Pro54=
NR_135776.2:n.546T>A
NR_135779.2:n.546T>A