Canonical Allele Identifier: CA406708750
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090545A>G (hg19) chr19:g.48587288A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587288A>G , CM000681.2:g.48587288A>G GRCh38
NC_000019.9:g.49090545A>G , CM000681.1:g.49090545A>G GRCh37
NC_000019.8:g.53782357A>G NCBI36
NG_029063.1:g.40117A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.274A>G MANE Select ENSP00000201586.2:p.Ile92Val
ENST00000201586.6:c.274A>G ENSP00000201586.1:p.Ile92Val
ENST00000323090.4:c.229A>G ENSP00000312880.3:p.Ile77Val
NM_004605.2:c.229A>G NP_004596.2:p.Ile77Val
NM_177973.1:c.274A>G NP_814444.1:p.Ile92Val
NM_177973.2:c.274A>G MANE Select NP_814444.1:p.Ile92Val
Search 100 bp 5'
Search 100 bp 3'