Canonical Allele Identifier: CA508042714

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090598T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587341T>G , CM000681.2:g.48587341T>G	GRCh38
NC_000019.9:g.49090598T>G , CM000681.1:g.49090598T>G	GRCh37
NC_000019.8:g.53782410T>G	NCBI36
NG_029063.1:g.40170T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.327T>G MANE Select	ENSP00000201586.2:p.Gly109=
ENST00000201586.6:c.327T>G	ENSP00000201586.1:p.Gly109=
ENST00000323090.4:c.282T>G	ENSP00000312880.3:p.Gly94=
NM_004605.2:c.282T>G	NP_004596.2:p.Gly94=
NM_177973.1:c.327T>G	NP_814444.1:p.Gly109=
NM_177973.2:c.327T>G MANE Select	NP_814444.1:p.Gly109=