Canonical Allele Identifier: CA348024011
Gene: SULT1C4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.108994824T>C (hg19) chr2:g.108378368T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378368T>C , CM000664.2:g.108378368T>C GRCh38
NC_000002.11:g.108994824T>C , CM000664.1:g.108994824T>C GRCh37
NC_000002.10:g.108361256T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.31T>C MANE Select ENSP00000272452.2:p.Phe11Leu
ENST00000272452.6:c.31T>C ENSP00000272452.2:p.Phe11Leu
ENST00000409309.3:c.31T>C ENSP00000387225.3:p.Phe11Leu
ENST00000494122.1:n.458T>C
NM_006588.2:c.31T>C NP_006579.2:p.Phe11Leu
XM_005263919.2:c.31T>C XP_005263976.1:p.Phe11Leu
NM_001321770.1:c.31T>C NP_001308699.1:p.Phe11Leu
NM_006588.3:c.31T>C NP_006579.2:p.Phe11Leu
NR_135776.1:n.458T>C
NR_135779.1:n.458T>C
NM_006588.4:c.31T>C MANE Select NP_006579.2:p.Phe11Leu
NM_001321770.2:c.31T>C NP_001308699.1:p.Phe11Leu
NR_135776.2:n.415T>C
NR_135779.2:n.415T>C
Search 100 bp 5'
Search 100 bp 3'