Canonical Allele Identifier: CA633602058
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1192756696
gnomAD v2: 19-49090933-T-G
gnomAD v3: 19-48587676-T-G
gnomAD v4: 19-48587676-T-G
MyVariant Identifiers: chr19:g.49090933T>G (hg19) chr19:g.48587676T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587676T>G , CM000681.2:g.48587676T>G GRCh38
NC_000019.9:g.49090933T>G , CM000681.1:g.49090933T>G GRCh37
NC_000019.8:g.53782745T>G NCBI36
NG_029063.1:g.40505T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+239T>G MANE Select ENSP00000201586.2:n.423+239T>G
ENST00000201586.6:c.423+239T>G ENSP00000201586.1:n.423+239T>G
ENST00000323090.4:c.378+239T>G ENSP00000312880.3:n.378+239T>G
NM_004605.2:c.378+239T>G NP_004596.2:n.378+239T>G
NM_177973.1:c.423+239T>G NP_814444.1:n.423+239T>G
NM_177973.2:c.423+239T>G MANE Select NP_814444.1:n.423+239T>G
Search 100 bp 5'
Search 100 bp 3'