Canonical Allele Identifier: CA2339970795
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587297G= , CM000681.2:g.48587297G= GRCh38
NC_000019.9:g.49090554G= , CM000681.1:g.49090554G= GRCh37
NC_000019.8:g.53782366G= NCBI36
NG_029063.1:g.40126G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.283G= MANE Select ENSP00000201586.2:p.Val95=
ENST00000201586.6:c.283G= ENSP00000201586.1:p.Val95=
ENST00000323090.4:c.238G= ENSP00000312880.3:p.Val80=
NM_004605.2:c.238G= NP_004596.2:p.Val80=
NM_177973.1:c.283G= NP_814444.1:p.Val95=
NM_177973.2:c.283G= MANE Select NP_814444.1:p.Val95=