Canonical Allele Identifier: CA53420344

Gene: SULT1C4

Linked Data

• dbSNP Id: rs200853144
• gnomAD v2: 2-108994768-G-C
• gnomAD v3: 2-108378312-G-C
• gnomAD v4: 2-108378312-G-C
• MyVariant Identifiers: chr2:g.108994768G>C (hg19) ; chr2:g.108378312G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378312G>C , CM000664.2:g.108378312G>C	GRCh38
NC_000002.11:g.108994768G>C , CM000664.1:g.108994768G>C	GRCh37
NC_000002.10:g.108361200G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.-26G>C MANE Select	ENSP00000272452.2:n.-26G>C
ENST00000272452.6:c.-26G>C	ENSP00000272452.2:n.-26G>C
ENST00000409309.3:c.-26G>C	ENSP00000387225.3:n.-26G>C
ENST00000494122.1:n.402G>C
NM_006588.2:c.-26G>C	NP_006579.2:n.-26G>C
XM_005263919.2:c.-26G>C	XP_005263976.1:n.-26G>C
NM_001321770.1:c.-26G>C	NP_001308699.1:n.-26G>C
NM_006588.3:c.-26G>C	NP_006579.2:n.-26G>C
NR_135776.1:n.402G>C
NR_135779.1:n.402G>C
NM_006588.4:c.-26G>C MANE Select	NP_006579.2:n.-26G>C
NM_001321770.2:c.-26G>C	NP_001308699.1:n.-26G>C
NR_135776.2:n.359G>C
NR_135779.2:n.359G>C