Canonical Allele Identifier: CA427904941

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1414699847
• gnomAD v2: 2-108994961-A-C
• gnomAD v4: 2-108378505-A-C
• MyVariant Identifiers: chr2:g.108994961A>C (hg19) ; chr2:g.108378505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378505A>C , CM000664.2:g.108378505A>C	GRCh38
NC_000002.11:g.108994961A>C , CM000664.1:g.108994961A>C	GRCh37
NC_000002.10:g.108361393A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.168A>C MANE Select	ENSP00000272452.2:p.Ala56=
ENST00000272452.6:c.168A>C	ENSP00000272452.2:p.Ala56=
ENST00000409309.3:c.168A>C	ENSP00000387225.3:p.Ala56=
ENST00000494122.1:n.595A>C
NM_006588.2:c.168A>C	NP_006579.2:p.Ala56=
XM_005263919.2:c.168A>C	XP_005263976.1:p.Ala56=
NM_001321770.1:c.168A>C	NP_001308699.1:p.Ala56=
NM_006588.3:c.168A>C	NP_006579.2:p.Ala56=
NR_135776.1:n.595A>C
NR_135779.1:n.595A>C
XM_017003807.1:c.-153A>C	XP_016859296.1:n.-153A>C
NM_006588.4:c.168A>C MANE Select	NP_006579.2:p.Ala56=
NM_001321770.2:c.168A>C	NP_001308699.1:p.Ala56=
NR_135776.2:n.552A>C
NR_135779.2:n.552A>C