Canonical Allele Identifier: CA2339970792
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587291C= , CM000681.2:g.48587291C= GRCh38
NC_000019.9:g.49090548C= , CM000681.1:g.49090548C= GRCh37
NC_000019.8:g.53782360C= NCBI36
NG_029063.1:g.40120C=

Transcript Alleles

HGVS Amino-acid change
ENST00000201586.7:c.277C= MANE Select ENSP00000201586.2:p.Arg93=
ENST00000201586.6:c.277C= ENSP00000201586.1:p.Arg93=
ENST00000323090.4:c.232C= ENSP00000312880.3:p.Arg78=
NM_004605.2:c.232C= NP_004596.2:p.Arg78=
NM_177973.1:c.277C= NP_814444.1:p.Arg93=
NM_177973.2:c.277C= MANE Select NP_814444.1:p.Arg93=