Canonical Allele Identifier: CA309383639
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs780820646
gnomAD v2: 19-49090617-C-T
gnomAD v3: 19-48587360-C-T
gnomAD v4: 19-48587360-C-T
COSMIC: COSM3701519 COSM3701520
MyVariant Identifiers: chr19:g.49090617C>T (hg19) chr19:g.48587360C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587360C>T , CM000681.2:g.48587360C>T GRCh38
NC_000019.9:g.49090617C>T , CM000681.1:g.49090617C>T GRCh37
NC_000019.8:g.53782429C>T NCBI36
NG_029063.1:g.40189C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.346C>T MANE Select ENSP00000201586.2:p.Gln116Ter
ENST00000201586.6:c.346C>T ENSP00000201586.1:p.Gln116Ter
ENST00000323090.4:c.301C>T ENSP00000312880.3:p.Gln101Ter
NM_004605.2:c.301C>T NP_004596.2:p.Gln101Ter
NM_177973.1:c.346C>T NP_814444.1:p.Gln116Ter
NM_177973.2:c.346C>T MANE Select NP_814444.1:p.Gln116Ter
Search 100 bp 5'
Search 100 bp 3'