Canonical Allele Identifier: CA9553061
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs766649000
ExAC: 19:49090712 G / A
gnomAD v2: 19-49090712-G-A
gnomAD v3: 19-48587455-G-A
gnomAD v4: 19-48587455-G-A
MyVariant Identifiers: chr19:g.49090712G>A (hg19) chr19:g.48587455G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587455G>A , CM000681.2:g.48587455G>A GRCh38
NC_000019.9:g.49090712G>A , CM000681.1:g.49090712G>A GRCh37
NC_000019.8:g.53782524G>A NCBI36
NG_029063.1:g.40284G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+18G>A MANE Select ENSP00000201586.2:n.423+18G>A
ENST00000201586.6:c.423+18G>A ENSP00000201586.1:n.423+18G>A
ENST00000323090.4:c.378+18G>A ENSP00000312880.3:n.378+18G>A
NM_004605.2:c.378+18G>A NP_004596.2:n.378+18G>A
NM_177973.1:c.423+18G>A NP_814444.1:n.423+18G>A
NM_177973.2:c.423+18G>A MANE Select NP_814444.1:n.423+18G>A
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