Canonical Allele Identifier: CA309383622

Gene: SULT2B1

Linked Data

• dbSNP Id: rs932416497
• MyVariant Identifiers: chr19:g.49090575C>T (hg19) ; chr19:g.48587318C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587318C>T , CM000681.2:g.48587318C>T	GRCh38
NC_000019.9:g.49090575C>T , CM000681.1:g.49090575C>T	GRCh37
NC_000019.8:g.53782387C>T	NCBI36
NG_029063.1:g.40147C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.304C>T MANE Select	ENSP00000201586.2:p.Pro102Ser
ENST00000201586.6:c.304C>T	ENSP00000201586.1:p.Pro102Ser
ENST00000323090.4:c.259C>T	ENSP00000312880.3:p.Pro87Ser
NM_004605.2:c.259C>T	NP_004596.2:p.Pro87Ser
NM_177973.1:c.304C>T	NP_814444.1:p.Pro102Ser
NM_177973.2:c.304C>T MANE Select	NP_814444.1:p.Pro102Ser