Canonical Allele Identifier: CA996611359
Gene: SULT2B1 HGNC NCBI

Linked Data

gnomAD v3: 19-48587662-C-CA
gnomAD v4: 19-48587662-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587662_48587663insA , CM000681.2:g.48587662_48587663insA GRCh38
NC_000019.9:g.49090919_49090920insA , CM000681.1:g.49090919_49090920insA GRCh37
NC_000019.8:g.53782731_53782732insA NCBI36
NG_029063.1:g.40491_40492insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+225_423+226insA MANE Select ENSP00000201586.2:n.423+225_423+226insA
ENST00000201586.6:c.423+225_423+226insA ENSP00000201586.1:n.423+225_423+226insA
ENST00000323090.4:c.378+225_378+226insA ENSP00000312880.3:n.378+225_378+226insA
NM_004605.2:c.378+225_378+226insA NP_004596.2:n.378+225_378+226insA
NM_177973.1:c.423+225_423+226insA NP_814444.1:n.423+225_423+226insA
NM_177973.2:c.423+225_423+226insA MANE Select NP_814444.1:n.423+225_423+226insA
Search 100 bp 5'
Search 100 bp 3'