Canonical Allele Identifier: CA1063867548
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs1721296763
gnomAD v3: 4-69858447-T-C
gnomAD v4: 4-69858447-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858447T>C , CM000666.2:g.69858447T>C GRCh38
NC_000004.11:g.70724165T>C , CM000666.1:g.70724165T>C GRCh37
NC_000004.10:g.70758754T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226444.4:c.-9-794A>G MANE Select ENSP00000226444.3:n.-9-794A>G
ENST00000226444.3:c.-9-794A>G ENSP00000226444.3:n.-9-794A>G
ENST00000504002.1:n.98-794A>G
NM_005420.2:c.-9-794A>G NP_005411.1:n.-9-794A>G
XM_011532209.1:c.-9-794A>G XP_011530511.1:n.-9-794A>G
XM_011532210.1:c.-9-794A>G XP_011530512.1:n.-9-794A>G
XM_011532210.2:c.-9-794A>G XP_011530512.1:n.-9-794A>G
NM_005420.3:c.-9-794A>G MANE Select NP_005411.1:n.-9-794A>G
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