Canonical Allele Identifier: CA53420321

Gene: SULT1C4

Linked Data

• dbSNP Id: rs958454389
• gnomAD v3: 2-108378275-C-T
• gnomAD v4: 2-108378275-C-T
• COSMIC: COSN513946
• MyVariant Identifiers: chr2:g.108994731C>T (hg19) ; chr2:g.108378275C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378275C>T , CM000664.2:g.108378275C>T	GRCh38
NC_000002.11:g.108994731C>T , CM000664.1:g.108994731C>T	GRCh37
NC_000002.10:g.108361163C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-63C>T MANE Select	ENSP00000272452.2:n.-63C>T
ENST00000272452.6:c.-63C>T	ENSP00000272452.2:n.-63C>T
ENST00000409309.3:c.-63C>T	ENSP00000387225.3:n.-63C>T
ENST00000494122.1:n.365C>T
NM_006588.2:c.-63C>T	NP_006579.2:n.-63C>T
XM_005263919.2:c.-63C>T	XP_005263976.1:n.-63C>T
NM_001321770.1:c.-63C>T	NP_001308699.1:n.-63C>T
NM_006588.3:c.-63C>T	NP_006579.2:n.-63C>T
NR_135776.1:n.365C>T
NR_135779.1:n.365C>T
NM_006588.4:c.-63C>T MANE Select	NP_006579.2:n.-63C>T
NM_001321770.2:c.-63C>T	NP_001308699.1:n.-63C>T
NR_135776.2:n.322C>T
NR_135779.2:n.322C>T