Canonical Allele Identifier: CA406709108
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090632C>A (hg19) chr19:g.48587375C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587375C>A , CM000681.2:g.48587375C>A GRCh38
NC_000019.9:g.49090632C>A , CM000681.1:g.49090632C>A GRCh37
NC_000019.8:g.53782444C>A NCBI36
NG_029063.1:g.40204C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.361C>A MANE Select ENSP00000201586.2:p.Leu121Ile
ENST00000201586.6:c.361C>A ENSP00000201586.1:p.Leu121Ile
ENST00000323090.4:c.316C>A ENSP00000312880.3:p.Leu106Ile
NM_004605.2:c.316C>A NP_004596.2:p.Leu106Ile
NM_177973.1:c.361C>A NP_814444.1:p.Leu121Ile
NM_177973.2:c.361C>A MANE Select NP_814444.1:p.Leu121Ile
Search 100 bp 5'
Search 100 bp 3'