Canonical Allele Identifier: CA882958381
Gene: SULT2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1217945529
gnomAD v3: 19-47881849-T-C
gnomAD v4: 19-47881849-T-C
MyVariant Identifiers: chr19:g.48385106T>C (hg19) chr19:g.47881849T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47881849T>C , CM000681.2:g.47881849T>C GRCh38
NC_000019.9:g.48385106T>C , CM000681.1:g.48385106T>C GRCh37
NC_000019.8:g.53076918T>C NCBI36
NG_016745.1:g.9549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222002.4:c.472+235A>G MANE Select ENSP00000222002.2:n.472+235A>G
ENST00000222002.3:c.472+235A>G ENSP00000222002.2:n.472+235A>G
NM_003167.3:c.472+235A>G NP_003158.2:n.472+235A>G
NM_003167.4:c.472+235A>G MANE Select NP_003158.2:n.472+235A>G
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