Canonical Allele Identifier: CA98903299
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs3822172
gnomAD v2: 4-70723840-C-T
gnomAD v3: 4-69858122-C-T
gnomAD v4: 4-69858122-C-T
MyVariant Identifiers: chr4:g.70723840C>T (hg19) chr4:g.69858122C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858122C>T , CM000666.2:g.69858122C>T GRCh38
NC_000004.11:g.70723840C>T , CM000666.1:g.70723840C>T GRCh37
NC_000004.10:g.70758429C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226444.4:c.-9-469G>A MANE Select ENSP00000226444.3:n.-9-469G>A
ENST00000226444.3:c.-9-469G>A ENSP00000226444.3:n.-9-469G>A
ENST00000504002.1:n.98-469G>A
NM_005420.2:c.-9-469G>A NP_005411.1:n.-9-469G>A
XM_011532209.1:c.-9-469G>A XP_011530511.1:n.-9-469G>A
XM_011532210.1:c.-9-469G>A XP_011530512.1:n.-9-469G>A
XM_011532210.2:c.-9-469G>A XP_011530512.1:n.-9-469G>A
NM_005420.3:c.-9-469G>A MANE Select NP_005411.1:n.-9-469G>A
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