Canonical Allele Identifier: CA882958385
Gene: SULT2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1317447094
gnomAD v3: 19-47881860-A-T
gnomAD v4: 19-47881860-A-T
MyVariant Identifiers: chr19:g.48385117A>T (hg19) chr19:g.47881860A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47881860A>T , CM000681.2:g.47881860A>T GRCh38
NC_000019.9:g.48385117A>T , CM000681.1:g.48385117A>T GRCh37
NC_000019.8:g.53076929A>T NCBI36
NG_016745.1:g.9538T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222002.4:c.472+224T>A MANE Select ENSP00000222002.2:n.472+224T>A
ENST00000222002.3:c.472+224T>A ENSP00000222002.2:n.472+224T>A
NM_003167.3:c.472+224T>A NP_003158.2:n.472+224T>A
NM_003167.4:c.472+224T>A MANE Select NP_003158.2:n.472+224T>A
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