Canonical Allele Identifier: CA633887666
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1249488636
gnomAD v2: 19-49090448-T-TC
gnomAD v3: 19-48587191-T-TC
gnomAD v4: 19-48587191-T-TC
MyVariant Identifiers: chr19:g.49090448_49090449insC (hg19) chr19:g.48587191_48587192insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587194dup , CM000681.2:g.48587194dup GRCh38
NC_000019.9:g.49090451dup , CM000681.1:g.49090451dup GRCh37
NC_000019.8:g.53782263dup NCBI36
NG_029063.1:g.40023dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.215-35dup MANE Select ENSP00000201586.2:n.215-35dup
ENST00000201586.6:c.215-35dup ENSP00000201586.1:n.215-35dup
ENST00000323090.4:c.170-35dup ENSP00000312880.3:n.170-35dup
NM_004605.2:c.170-35dup NP_004596.2:n.170-35dup
NM_177973.1:c.215-35dup NP_814444.1:n.215-35dup
NM_177973.2:c.215-35dup MANE Select NP_814444.1:n.215-35dup
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Search 100 bp 3'