Canonical Allele Identifier: CA882958370
Gene: SULT2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1482670579
MyVariant Identifiers: chr19:g.48385094C>A (hg19) chr19:g.47881837C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47881837C>A , CM000681.2:g.47881837C>A GRCh38
NC_000019.9:g.48385094C>A , CM000681.1:g.48385094C>A GRCh37
NC_000019.8:g.53076906C>A NCBI36
NG_016745.1:g.9561G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222002.4:c.472+247G>T MANE Select ENSP00000222002.2:n.472+247G>T
ENST00000222002.3:c.472+247G>T ENSP00000222002.2:n.472+247G>T
NM_003167.3:c.472+247G>T NP_003158.2:n.472+247G>T
NM_003167.4:c.472+247G>T MANE Select NP_003158.2:n.472+247G>T
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