Canonical Allele Identifier: CA2736103742
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs2147622556

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587619T>C , CM000681.2:g.48587619T>C GRCh38
NC_000019.9:g.49090876T>C , CM000681.1:g.49090876T>C GRCh37
NC_000019.8:g.53782688T>C NCBI36
NG_029063.1:g.40448T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+182T>C MANE Select ENSP00000201586.2:n.423+182T>C
ENST00000201586.6:c.423+182T>C ENSP00000201586.1:n.423+182T>C
ENST00000323090.4:c.378+182T>C ENSP00000312880.3:n.378+182T>C
NM_004605.2:c.378+182T>C NP_004596.2:n.378+182T>C
NM_177973.1:c.423+182T>C NP_814444.1:n.423+182T>C
NM_177973.2:c.423+182T>C MANE Select NP_814444.1:n.423+182T>C