Canonical Allele Identifier: CA2339970936
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1973583483

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587646C>T , CM000681.2:g.48587646C>T GRCh38
NC_000019.9:g.49090903C>T , CM000681.1:g.49090903C>T GRCh37
NC_000019.8:g.53782715C>T NCBI36
NG_029063.1:g.40475C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+209C>T MANE Select ENSP00000201586.2:n.423+209C>T
ENST00000201586.6:c.423+209C>T ENSP00000201586.1:n.423+209C>T
ENST00000323090.4:c.378+209C>T ENSP00000312880.3:n.378+209C>T
NM_004605.2:c.378+209C>T NP_004596.2:n.378+209C>T
NM_177973.1:c.423+209C>T NP_814444.1:n.423+209C>T
NM_177973.2:c.423+209C>T MANE Select NP_814444.1:n.423+209C>T