Canonical Allele Identifier: CA508042720

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090601C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587344C>A , CM000681.2:g.48587344C>A	GRCh38
NC_000019.9:g.49090601C>A , CM000681.1:g.49090601C>A	GRCh37
NC_000019.8:g.53782413C>A	NCBI36
NG_029063.1:g.40173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.330C>A MANE Select	ENSP00000201586.2:p.Ala110=
ENST00000201586.6:c.330C>A	ENSP00000201586.1:p.Ala110=
ENST00000323090.4:c.285C>A	ENSP00000312880.3:p.Ala95=
NM_004605.2:c.285C>A	NP_004596.2:p.Ala95=
NM_177973.1:c.330C>A	NP_814444.1:p.Ala110=
NM_177973.2:c.330C>A MANE Select	NP_814444.1:p.Ala110=