Canonical Allele Identifier: CA406708789
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090555T>A (hg19) chr19:g.48587298T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587298T>A , CM000681.2:g.48587298T>A GRCh38
NC_000019.9:g.49090555T>A , CM000681.1:g.49090555T>A GRCh37
NC_000019.8:g.53782367T>A NCBI36
NG_029063.1:g.40127T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.284T>A MANE Select ENSP00000201586.2:p.Val95Glu
ENST00000201586.6:c.284T>A ENSP00000201586.1:p.Val95Glu
ENST00000323090.4:c.239T>A ENSP00000312880.3:p.Val80Glu
NM_004605.2:c.239T>A NP_004596.2:p.Val80Glu
NM_177973.1:c.284T>A NP_814444.1:p.Val95Glu
NM_177973.2:c.284T>A MANE Select NP_814444.1:p.Val95Glu
Search 100 bp 5'
Search 100 bp 3'