Canonical Allele Identifier: CA508042628

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090538A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587281A>C , CM000681.2:g.48587281A>C	GRCh38
NC_000019.9:g.49090538A>C , CM000681.1:g.49090538A>C	GRCh37
NC_000019.8:g.53782350A>C	NCBI36
NG_029063.1:g.40110A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.267A>C MANE Select	ENSP00000201586.2:p.Pro89=
ENST00000201586.6:c.267A>C	ENSP00000201586.1:p.Pro89=
ENST00000323090.4:c.222A>C	ENSP00000312880.3:p.Pro74=
NM_004605.2:c.222A>C	NP_004596.2:p.Pro74=
NM_177973.1:c.267A>C	NP_814444.1:p.Pro89=
NM_177973.2:c.267A>C MANE Select	NP_814444.1:p.Pro89=