Canonical Allele Identifier: CA2339970839
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587430A= , CM000681.2:g.48587430A= GRCh38
NC_000019.9:g.49090687A= , CM000681.1:g.49090687A= GRCh37
NC_000019.8:g.53782499A= NCBI36
NG_029063.1:g.40259A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.416A= MANE Select ENSP00000201586.2:p.Lys139=
ENST00000201586.6:c.416A= ENSP00000201586.1:p.Lys139=
ENST00000323090.4:c.371A= ENSP00000312880.3:p.Lys124=
NM_004605.2:c.371A= NP_004596.2:p.Lys124=
NM_177973.1:c.416A= NP_814444.1:p.Lys139=
NM_177973.2:c.416A= MANE Select NP_814444.1:p.Lys139=