Canonical Allele Identifier: CA1034796227
Gene: SULT1C4 HGNC NCBI

Linked Data

dbSNP Id: rs958454389

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378275C>G , CM000664.2:g.108378275C>G GRCh38
NC_000002.11:g.108994731C>G , CM000664.1:g.108994731C>G GRCh37
NC_000002.10:g.108361163C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-63C>G MANE Select ENSP00000272452.2:n.-63C>G
ENST00000272452.6:c.-63C>G ENSP00000272452.2:n.-63C>G
ENST00000409309.3:c.-63C>G ENSP00000387225.3:n.-63C>G
ENST00000494122.1:n.365C>G
NM_006588.2:c.-63C>G NP_006579.2:n.-63C>G
XM_005263919.2:c.-63C>G XP_005263976.1:n.-63C>G
NM_001321770.1:c.-63C>G NP_001308699.1:n.-63C>G
NM_006588.3:c.-63C>G NP_006579.2:n.-63C>G
NR_135776.1:n.365C>G
NR_135779.1:n.365C>G
NM_006588.4:c.-63C>G MANE Select NP_006579.2:n.-63C>G
NM_001321770.2:c.-63C>G NP_001308699.1:n.-63C>G
NR_135776.2:n.322C>G
NR_135779.2:n.322C>G