Canonical Allele Identifier: CA9553042
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs138292714
ExAC: 19:49090570 G / A
gnomAD v2: 19-49090570-G-A
gnomAD v3: 19-48587313-G-A
gnomAD v4: 19-48587313-G-A
MyVariant Identifiers: chr19:g.49090570G>A (hg19) chr19:g.48587313G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587313G>A , CM000681.2:g.48587313G>A GRCh38
NC_000019.9:g.49090570G>A , CM000681.1:g.49090570G>A GRCh37
NC_000019.8:g.53782382G>A NCBI36
NG_029063.1:g.40142G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.299G>A MANE Select ENSP00000201586.2:p.Arg100Gln
ENST00000201586.6:c.299G>A ENSP00000201586.1:p.Arg100Gln
ENST00000323090.4:c.254G>A ENSP00000312880.3:p.Arg85Gln
NM_004605.2:c.254G>A NP_004596.2:p.Arg85Gln
NM_177973.1:c.299G>A NP_814444.1:p.Arg100Gln
NM_177973.2:c.299G>A MANE Select NP_814444.1:p.Arg100Gln
Search 100 bp 5'
Search 100 bp 3'