Canonical Allele Identifier: CA348024021

Gene: SULT1C4

Linked Data

• dbSNP Id: rs2104338119
• MyVariant Identifiers: chr2:g.108994827G>C (hg19) ; chr2:g.108378371G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378371G>C , CM000664.2:g.108378371G>C	GRCh38
NC_000002.11:g.108994827G>C , CM000664.1:g.108994827G>C	GRCh37
NC_000002.10:g.108361259G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.34G>C MANE Select	ENSP00000272452.2:p.Asp12His
ENST00000272452.6:c.34G>C	ENSP00000272452.2:p.Asp12His
ENST00000409309.3:c.34G>C	ENSP00000387225.3:p.Asp12His
ENST00000494122.1:n.461G>C
NM_006588.2:c.34G>C	NP_006579.2:p.Asp12His
XM_005263919.2:c.34G>C	XP_005263976.1:p.Asp12His
NM_001321770.1:c.34G>C	NP_001308699.1:p.Asp12His
NM_006588.3:c.34G>C	NP_006579.2:p.Asp12His
NR_135776.1:n.461G>C
NR_135779.1:n.461G>C
NM_006588.4:c.34G>C MANE Select	NP_006579.2:p.Asp12His
NM_001321770.2:c.34G>C	NP_001308699.1:p.Asp12His
NR_135776.2:n.418G>C
NR_135779.2:n.418G>C