Canonical Allele Identifier: CA508042634
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090541C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587284C>A , CM000681.2:g.48587284C>A GRCh38
NC_000019.9:g.49090541C>A , CM000681.1:g.49090541C>A GRCh37
NC_000019.8:g.53782353C>A NCBI36
NG_029063.1:g.40113C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000201586.7:c.270C>A MANE Select ENSP00000201586.2:p.Ser90=
ENST00000201586.6:c.270C>A ENSP00000201586.1:p.Ser90=
ENST00000323090.4:c.225C>A ENSP00000312880.3:p.Ser75=
NM_004605.2:c.225C>A NP_004596.2:p.Ser75=
NM_177973.1:c.270C>A NP_814444.1:p.Ser90=
NM_177973.2:c.270C>A MANE Select NP_814444.1:p.Ser90=
Search 100 bp 5'
Search 100 bp 3'