Canonical Allele Identifier: CA1819935
Gene: SULT1C4 HGNC NCBI

Linked Data

dbSNP Id: rs775290089

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378483T>C , CM000664.2:g.108378483T>C GRCh38
NC_000002.11:g.108994939T>C , CM000664.1:g.108994939T>C GRCh37
NC_000002.10:g.108361371T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.146T>C MANE Select ENSP00000272452.2:p.Leu49Pro
ENST00000272452.6:c.146T>C ENSP00000272452.2:p.Leu49Pro
ENST00000409309.3:c.146T>C ENSP00000387225.3:p.Leu49Pro
ENST00000494122.1:n.573T>C
NM_006588.2:c.146T>C NP_006579.2:p.Leu49Pro
XM_005263919.2:c.146T>C XP_005263976.1:p.Leu49Pro
NM_001321770.1:c.146T>C NP_001308699.1:p.Leu49Pro
NM_006588.3:c.146T>C NP_006579.2:p.Leu49Pro
NR_135776.1:n.573T>C
NR_135779.1:n.573T>C
XM_017003807.1:c.-175T>C XP_016859296.1:n.-175T>C
NM_006588.4:c.146T>C MANE Select NP_006579.2:p.Leu49Pro
NM_001321770.2:c.146T>C NP_001308699.1:p.Leu49Pro
NR_135776.2:n.530T>C
NR_135779.2:n.530T>C