Canonical Allele Identifier: CA508042676

Gene: SULT2B1

Linked Data

• MyVariant Identifiers: chr19:g.49090571G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587314G>C , CM000681.2:g.48587314G>C	GRCh38
NC_000019.9:g.49090571G>C , CM000681.1:g.49090571G>C	GRCh37
NC_000019.8:g.53782383G>C	NCBI36
NG_029063.1:g.40143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.300G>C MANE Select	ENSP00000201586.2:p.Arg100=
ENST00000201586.6:c.300G>C	ENSP00000201586.1:p.Arg100=
ENST00000323090.4:c.255G>C	ENSP00000312880.3:p.Arg85=
NM_004605.2:c.255G>C	NP_004596.2:p.Arg85=
NM_177973.1:c.300G>C	NP_814444.1:p.Arg100=
NM_177973.2:c.300G>C MANE Select	NP_814444.1:p.Arg100=