Canonical Allele Identifier: CA309236916
Gene: SULT2A1 HGNC NCBI

Linked Data

dbSNP Id: rs963724649
gnomAD v2: 19-48385063-G-A
gnomAD v3: 19-47881806-G-A
gnomAD v4: 19-47881806-G-A
MyVariant Identifiers: chr19:g.48385063G>A (hg19) chr19:g.47881806G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47881806G>A , CM000681.2:g.47881806G>A GRCh38
NC_000019.9:g.48385063G>A , CM000681.1:g.48385063G>A GRCh37
NC_000019.8:g.53076875G>A NCBI36
NG_016745.1:g.9592C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222002.4:c.472+278C>T MANE Select ENSP00000222002.2:n.472+278C>T
ENST00000222002.3:c.472+278C>T ENSP00000222002.2:n.472+278C>T
NM_003167.3:c.472+278C>T NP_003158.2:n.472+278C>T
NM_003167.4:c.472+278C>T MANE Select NP_003158.2:n.472+278C>T
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