Canonical Allele Identifier: CA2339970929
Gene: SULT2B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587627C= , CM000681.2:g.48587627C= GRCh38
NC_000019.9:g.49090884C= , CM000681.1:g.49090884C= GRCh37
NC_000019.8:g.53782696C= NCBI36
NG_029063.1:g.40456C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+190C= MANE Select ENSP00000201586.2:n.423+190C=
ENST00000201586.6:c.423+190C= ENSP00000201586.1:n.423+190C=
ENST00000323090.4:c.378+190C= ENSP00000312880.3:n.378+190C=
NM_004605.2:c.378+190C= NP_004596.2:n.378+190C=
NM_177973.1:c.423+190C= NP_814444.1:n.423+190C=
NM_177973.2:c.423+190C= MANE Select NP_814444.1:n.423+190C=
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