Canonical Allele Identifier: CA406708636
Gene: SULT2B1 HGNC NCBI

Linked Data

gnomAD v4: 19-48587262-T-A
MyVariant Identifiers: chr19:g.49090519T>A (hg19) chr19:g.48587262T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587262T>A , CM000681.2:g.48587262T>A GRCh38
NC_000019.9:g.49090519T>A , CM000681.1:g.49090519T>A GRCh37
NC_000019.8:g.53782331T>A NCBI36
NG_029063.1:g.40091T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.248T>A MANE Select ENSP00000201586.2:p.Ile83Asn
ENST00000201586.6:c.248T>A ENSP00000201586.1:p.Ile83Asn
ENST00000323090.4:c.203T>A ENSP00000312880.3:p.Ile68Asn
NM_004605.2:c.203T>A NP_004596.2:p.Ile68Asn
NM_177973.1:c.248T>A NP_814444.1:p.Ile83Asn
NM_177973.2:c.248T>A MANE Select NP_814444.1:p.Ile83Asn
Search 100 bp 5'
Search 100 bp 3'