Canonical Allele Identifier: CA1063867547
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs1721296053
gnomAD v3: 4-69858440-C-A
gnomAD v4: 4-69858440-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858440C>A , CM000666.2:g.69858440C>A GRCh38
NC_000004.11:g.70724158C>A , CM000666.1:g.70724158C>A GRCh37
NC_000004.10:g.70758747C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226444.4:c.-9-787G>T MANE Select ENSP00000226444.3:n.-9-787G>T
ENST00000226444.3:c.-9-787G>T ENSP00000226444.3:n.-9-787G>T
ENST00000504002.1:n.98-787G>T
NM_005420.2:c.-9-787G>T NP_005411.1:n.-9-787G>T
XM_011532209.1:c.-9-787G>T XP_011530511.1:n.-9-787G>T
XM_011532210.1:c.-9-787G>T XP_011530512.1:n.-9-787G>T
XM_011532210.2:c.-9-787G>T XP_011530512.1:n.-9-787G>T
NM_005420.3:c.-9-787G>T MANE Select NP_005411.1:n.-9-787G>T