Canonical Allele Identifier: CA98903579
Gene: SULT1E1 HGNC NCBI

Linked Data

dbSNP Id: rs976577734
gnomAD v2: 4-70724161-T-A
gnomAD v3: 4-69858443-T-A
gnomAD v4: 4-69858443-T-A
MyVariant Identifiers: chr4:g.70724161T>A (hg19) chr4:g.69858443T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69858443T>A , CM000666.2:g.69858443T>A GRCh38
NC_000004.11:g.70724161T>A , CM000666.1:g.70724161T>A GRCh37
NC_000004.10:g.70758750T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226444.4:c.-9-790A>T MANE Select ENSP00000226444.3:n.-9-790A>T
ENST00000226444.3:c.-9-790A>T ENSP00000226444.3:n.-9-790A>T
ENST00000504002.1:n.98-790A>T
NM_005420.2:c.-9-790A>T NP_005411.1:n.-9-790A>T
XM_011532209.1:c.-9-790A>T XP_011530511.1:n.-9-790A>T
XM_011532210.1:c.-9-790A>T XP_011530512.1:n.-9-790A>T
XM_011532210.2:c.-9-790A>T XP_011530512.1:n.-9-790A>T
NM_005420.3:c.-9-790A>T MANE Select NP_005411.1:n.-9-790A>T
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