Canonical Allele Identifier: CA98903288
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs1005979374
MyVariant Identifiers: chr4:g.70723834T>G (hg19) chr4:g.69858116T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858116T>G , CM000666.2:g.69858116T>G GRCh38
NC_000004.11:g.70723834T>G , CM000666.1:g.70723834T>G GRCh37
NC_000004.10:g.70758423T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226444.4:c.-9-463A>C MANE Select ENSP00000226444.3:n.-9-463A>C
ENST00000226444.3:c.-9-463A>C ENSP00000226444.3:n.-9-463A>C
ENST00000504002.1:n.98-463A>C
NM_005420.2:c.-9-463A>C NP_005411.1:n.-9-463A>C
XM_011532209.1:c.-9-463A>C XP_011530511.1:n.-9-463A>C
XM_011532210.1:c.-9-463A>C XP_011530512.1:n.-9-463A>C
XM_011532210.2:c.-9-463A>C XP_011530512.1:n.-9-463A>C
NM_005420.3:c.-9-463A>C MANE Select NP_005411.1:n.-9-463A>C
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