Canonical Allele Identifier: CA406709127
Gene: SULT2B1 HGNC NCBI

Linked Data

gnomAD v4: 19-48587380-G-A
MyVariant Identifiers: chr19:g.49090637G>A (hg19) chr19:g.48587380G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587380G>A , CM000681.2:g.48587380G>A GRCh38
NC_000019.9:g.49090637G>A , CM000681.1:g.49090637G>A GRCh37
NC_000019.8:g.53782449G>A NCBI36
NG_029063.1:g.40209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.366G>A MANE Select ENSP00000201586.2:p.Met122Ile
ENST00000201586.6:c.366G>A ENSP00000201586.1:p.Met122Ile
ENST00000323090.4:c.321G>A ENSP00000312880.3:p.Met107Ile
NM_004605.2:c.321G>A NP_004596.2:p.Met107Ile
NM_177973.1:c.366G>A NP_814444.1:p.Met122Ile
NM_177973.2:c.366G>A MANE Select NP_814444.1:p.Met122Ile
Search 100 bp 5'
Search 100 bp 3'