Canonical Allele Identifier: CA633602057
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1475405413
gnomAD v2: 19-49090924-G-A
gnomAD v3: 19-48587667-G-A
gnomAD v4: 19-48587667-G-A
MyVariant Identifiers: chr19:g.49090924G>A (hg19) chr19:g.48587667G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587667G>A , CM000681.2:g.48587667G>A GRCh38
NC_000019.9:g.49090924G>A , CM000681.1:g.49090924G>A GRCh37
NC_000019.8:g.53782736G>A NCBI36
NG_029063.1:g.40496G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+230G>A MANE Select ENSP00000201586.2:n.423+230G>A
ENST00000201586.6:c.423+230G>A ENSP00000201586.1:n.423+230G>A
ENST00000323090.4:c.378+230G>A ENSP00000312880.3:n.378+230G>A
NM_004605.2:c.378+230G>A NP_004596.2:n.378+230G>A
NM_177973.1:c.423+230G>A NP_814444.1:n.423+230G>A
NM_177973.2:c.423+230G>A MANE Select NP_814444.1:n.423+230G>A
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