Canonical Allele Identifier: CA406709192
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090648T>A (hg19) chr19:g.48587391T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587391T>A , CM000681.2:g.48587391T>A GRCh38
NC_000019.9:g.49090648T>A , CM000681.1:g.49090648T>A GRCh37
NC_000019.8:g.53782460T>A NCBI36
NG_029063.1:g.40220T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.377T>A MANE Select ENSP00000201586.2:p.Leu126His
ENST00000201586.6:c.377T>A ENSP00000201586.1:p.Leu126His
ENST00000323090.4:c.332T>A ENSP00000312880.3:p.Leu111His
NM_004605.2:c.332T>A NP_004596.2:p.Leu111His
NM_177973.1:c.377T>A NP_814444.1:p.Leu126His
NM_177973.2:c.377T>A MANE Select NP_814444.1:p.Leu126His
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