Canonical Allele Identifier: CA2339970772
Gene: SULT2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587225A= , CM000681.2:g.48587225A= GRCh38
NC_000019.9:g.49090482A= , CM000681.1:g.49090482A= GRCh37
NC_000019.8:g.53782294A= NCBI36
NG_029063.1:g.40054A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.215-4A= MANE Select ENSP00000201586.2:n.215-4A=
ENST00000201586.6:c.215-4A= ENSP00000201586.1:n.215-4A=
ENST00000323090.4:c.170-4A= ENSP00000312880.3:n.170-4A=
NM_004605.2:c.170-4A= NP_004596.2:n.170-4A=
NM_177973.1:c.215-4A= NP_814444.1:n.215-4A=
NM_177973.2:c.215-4A= MANE Select NP_814444.1:n.215-4A=