Canonical Allele Identifier: CA348024357

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1678302890
• MyVariant Identifiers: chr2:g.108994911A>T (hg19) ; chr2:g.108378455A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378455A>T , CM000664.2:g.108378455A>T	GRCh38
NC_000002.11:g.108994911A>T , CM000664.1:g.108994911A>T	GRCh37
NC_000002.10:g.108361343A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.118A>T MANE Select	ENSP00000272452.2:p.Asn40Tyr
ENST00000272452.6:c.118A>T	ENSP00000272452.2:p.Asn40Tyr
ENST00000409309.3:c.118A>T	ENSP00000387225.3:p.Asn40Tyr
ENST00000494122.1:n.545A>T
NM_006588.2:c.118A>T	NP_006579.2:p.Asn40Tyr
XM_005263919.2:c.118A>T	XP_005263976.1:p.Asn40Tyr
NM_001321770.1:c.118A>T	NP_001308699.1:p.Asn40Tyr
NM_006588.3:c.118A>T	NP_006579.2:p.Asn40Tyr
NR_135776.1:n.545A>T
NR_135779.1:n.545A>T
XM_017003807.1:c.-203A>T	XP_016859296.1:n.-203A>T
NM_006588.4:c.118A>T MANE Select	NP_006579.2:p.Asn40Tyr
NM_001321770.2:c.118A>T	NP_001308699.1:p.Asn40Tyr
NR_135776.2:n.502A>T
NR_135779.2:n.502A>T