Canonical Allele Identifier: CA2339970787
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587279C= , CM000681.2:g.48587279C= GRCh38
NC_000019.9:g.49090536C= , CM000681.1:g.49090536C= GRCh37
NC_000019.8:g.53782348C= NCBI36
NG_029063.1:g.40108C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.265C= MANE Select ENSP00000201586.2:p.Pro89=
ENST00000201586.6:c.265C= ENSP00000201586.1:p.Pro89=
ENST00000323090.4:c.220C= ENSP00000312880.3:p.Pro74=
NM_004605.2:c.220C= NP_004596.2:p.Pro74=
NM_177973.1:c.265C= NP_814444.1:p.Pro89=
NM_177973.2:c.265C= MANE Select NP_814444.1:p.Pro89=