Canonical Allele Identifier: CA1819915

Gene: SULT1C4

Linked Data

• ClinVar Variation Id: 2457300
• ClinVar RCV Id: RCV004254430
• dbSNP Id: rs759448103
• ExAC: 2:108994803 C / T
• gnomAD v2: 2-108994803-C-T
• gnomAD v4: 2-108378347-C-T
• MyVariant Identifiers: chr2:g.108994803C>T (hg19) ; chr2:g.108378347C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378347C>T , CM000664.2:g.108378347C>T	GRCh38
NC_000002.11:g.108994803C>T , CM000664.1:g.108994803C>T	GRCh37
NC_000002.10:g.108361235C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.10C>T MANE Select	ENSP00000272452.2:p.His4Tyr
ENST00000272452.6:c.10C>T	ENSP00000272452.2:p.His4Tyr
ENST00000409309.3:c.10C>T	ENSP00000387225.3:p.His4Tyr
ENST00000494122.1:n.437C>T
NM_006588.2:c.10C>T	NP_006579.2:p.His4Tyr
XM_005263919.2:c.10C>T	XP_005263976.1:p.His4Tyr
NM_001321770.1:c.10C>T	NP_001308699.1:p.His4Tyr
NM_006588.3:c.10C>T	NP_006579.2:p.His4Tyr
NR_135776.1:n.437C>T
NR_135779.1:n.437C>T
NM_006588.4:c.10C>T MANE Select	NP_006579.2:p.His4Tyr
NM_001321770.2:c.10C>T	NP_001308699.1:p.His4Tyr
NR_135776.2:n.394C>T
NR_135779.2:n.394C>T