Canonical Allele Identifier: CA2339970861
Gene: SULT2B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587484A= , CM000681.2:g.48587484A= GRCh38
NC_000019.9:g.49090741A= , CM000681.1:g.49090741A= GRCh37
NC_000019.8:g.53782553A= NCBI36
NG_029063.1:g.40313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+47A= MANE Select ENSP00000201586.2:n.423+47A=
ENST00000201586.6:c.423+47A= ENSP00000201586.1:n.423+47A=
ENST00000323090.4:c.378+47A= ENSP00000312880.3:n.378+47A=
NM_004605.2:c.378+47A= NP_004596.2:n.378+47A=
NM_177973.1:c.423+47A= NP_814444.1:n.423+47A=
NM_177973.2:c.423+47A= MANE Select NP_814444.1:n.423+47A=
Search 100 bp 5'
Search 100 bp 3'