Canonical Allele Identifier: CA2339970788
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587280C= , CM000681.2:g.48587280C= GRCh38
NC_000019.9:g.49090537C= , CM000681.1:g.49090537C= GRCh37
NC_000019.8:g.53782349C= NCBI36
NG_029063.1:g.40109C=

Transcript Alleles

HGVS Amino-acid change
ENST00000201586.7:c.266C= MANE Select ENSP00000201586.2:p.Pro89=
ENST00000201586.6:c.266C= ENSP00000201586.1:p.Pro89=
ENST00000323090.4:c.221C= ENSP00000312880.3:p.Pro74=
NM_004605.2:c.221C= NP_004596.2:p.Pro74=
NM_177973.1:c.266C= NP_814444.1:p.Pro89=
NM_177973.2:c.266C= MANE Select NP_814444.1:p.Pro89=