Canonical Allele Identifier: CA508042725

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090604C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587347C>T , CM000681.2:g.48587347C>T	GRCh38
NC_000019.9:g.49090604C>T , CM000681.1:g.49090604C>T	GRCh37
NC_000019.8:g.53782416C>T	NCBI36
NG_029063.1:g.40176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.333C>T MANE Select	ENSP00000201586.2:p.Phe111=
ENST00000201586.6:c.333C>T	ENSP00000201586.1:p.Phe111=
ENST00000323090.4:c.288C>T	ENSP00000312880.3:p.Phe96=
NM_004605.2:c.288C>T	NP_004596.2:p.Phe96=
NM_177973.1:c.333C>T	NP_814444.1:p.Phe111=
NM_177973.2:c.333C>T MANE Select	NP_814444.1:p.Phe111=