Canonical Allele Identifier: CA2586212543
Gene: SULT2B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587452dup , CM000681.2:g.48587452dup GRCh38
NC_000019.9:g.49090709dup , CM000681.1:g.49090709dup GRCh37
NC_000019.8:g.53782521dup NCBI36
NG_029063.1:g.40281dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+15dup MANE Select ENSP00000201586.2:n.423+15dup
ENST00000201586.6:c.423+15dup ENSP00000201586.1:n.423+15dup
ENST00000323090.4:c.378+15dup ENSP00000312880.3:n.378+15dup
NM_004605.2:c.378+15dup NP_004596.2:n.378+15dup
NM_177973.1:c.423+15dup NP_814444.1:n.423+15dup
NM_177973.2:c.423+15dup MANE Select NP_814444.1:n.423+15dup