Canonical Allele Identifier: CA508042798

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090694G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587437G>A , CM000681.2:g.48587437G>A	GRCh38
NC_000019.9:g.49090694G>A , CM000681.1:g.49090694G>A	GRCh37
NC_000019.8:g.53782506G>A	NCBI36
NG_029063.1:g.40266G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.423G>A MANE Select	ENSP00000201586.2:p.Lys141=
ENST00000201586.6:c.423G>A	ENSP00000201586.1:p.Lys141=
ENST00000323090.4:c.378G>A	ENSP00000312880.3:p.Lys126=
NM_004605.2:c.378G>A	NP_004596.2:p.Lys126=
NM_177973.1:c.423G>A	NP_814444.1:p.Lys141=
NM_177973.2:c.423G>A MANE Select	NP_814444.1:p.Lys141=