Canonical Allele Identifier: CA406709297

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090665A>G (hg19) ; chr19:g.48587408A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587408A>G , CM000681.2:g.48587408A>G	GRCh38
NC_000019.9:g.49090665A>G , CM000681.1:g.49090665A>G	GRCh37
NC_000019.8:g.53782477A>G	NCBI36
NG_029063.1:g.40237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.394A>G MANE Select	ENSP00000201586.2:p.Thr132Ala
ENST00000201586.6:c.394A>G	ENSP00000201586.1:p.Thr132Ala
ENST00000323090.4:c.349A>G	ENSP00000312880.3:p.Thr117Ala
NM_004605.2:c.349A>G	NP_004596.2:p.Thr117Ala
NM_177973.1:c.394A>G	NP_814444.1:p.Thr132Ala
NM_177973.2:c.394A>G MANE Select	NP_814444.1:p.Thr132Ala