Canonical Allele Identifier: CA508042764

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090643C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587386C>A , CM000681.2:g.48587386C>A	GRCh38
NC_000019.9:g.49090643C>A , CM000681.1:g.49090643C>A	GRCh37
NC_000019.8:g.53782455C>A	NCBI36
NG_029063.1:g.40215C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.372C>A MANE Select	ENSP00000201586.2:p.Ser124=
ENST00000201586.6:c.372C>A	ENSP00000201586.1:p.Ser124=
ENST00000323090.4:c.327C>A	ENSP00000312880.3:p.Ser109=
NM_004605.2:c.327C>A	NP_004596.2:p.Ser109=
NM_177973.1:c.372C>A	NP_814444.1:p.Ser124=
NM_177973.2:c.372C>A MANE Select	NP_814444.1:p.Ser124=