Canonical Allele Identifier: CA309236929
Gene: SULT2A1 HGNC NCBI

Linked Data

dbSNP Id: rs955192947
gnomAD v2: 19-48385086-A-G
gnomAD v3: 19-47881829-A-G
gnomAD v4: 19-47881829-A-G
MyVariant Identifiers: chr19:g.48385086A>G (hg19) chr19:g.47881829A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47881829A>G , CM000681.2:g.47881829A>G GRCh38
NC_000019.9:g.48385086A>G , CM000681.1:g.48385086A>G GRCh37
NC_000019.8:g.53076898A>G NCBI36
NG_016745.1:g.9569T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222002.4:c.472+255T>C MANE Select ENSP00000222002.2:n.472+255T>C
ENST00000222002.3:c.472+255T>C ENSP00000222002.2:n.472+255T>C
NM_003167.3:c.472+255T>C NP_003158.2:n.472+255T>C
NM_003167.4:c.472+255T>C MANE Select NP_003158.2:n.472+255T>C
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