Canonical Allele Identifier: CA2339970789
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587282T= , CM000681.2:g.48587282T= GRCh38
NC_000019.9:g.49090539T= , CM000681.1:g.49090539T= GRCh37
NC_000019.8:g.53782351T= NCBI36
NG_029063.1:g.40111T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.268T= MANE Select ENSP00000201586.2:p.Ser90=
ENST00000201586.6:c.268T= ENSP00000201586.1:p.Ser90=
ENST00000323090.4:c.223T= ENSP00000312880.3:p.Ser75=
NM_004605.2:c.223T= NP_004596.2:p.Ser75=
NM_177973.1:c.268T= NP_814444.1:p.Ser90=
NM_177973.2:c.268T= MANE Select NP_814444.1:p.Ser90=