Canonical Allele Identifier: CA309383780
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs543951587
gnomAD v2: 19-49090875-GT-G
gnomAD v3: 19-48587618-GT-G
gnomAD v4: 19-48587618-GT-G
MyVariant Identifiers: chr19:g.49090876del (hg19) chr19:g.48587619del (hg38)
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Genomic Alleles

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

Transcript Alleles

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