Canonical Allele Identifier: CA470283984

Gene: CHST3

Linked Data

• MyVariant Identifiers: chr10:g.73767617C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007859C>G , CM000672.2:g.72007859C>G	GRCh38
NC_000010.10:g.73767617C>G , CM000672.1:g.73767617C>G	GRCh37
NC_000010.9:g.73437623C>G	NCBI36
NG_012635.1:g.48498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.828C>G MANE Select	ENSP00000362207.4:p.Arg276=
ENST00000373115.4:c.828C>G	ENSP00000362207.4:p.Arg276=
NM_004273.4:c.828C>G	NP_004264.2:p.Arg276=
XM_006718075.2:c.828C>G	XP_006718138.1:p.Arg276=
XM_011540369.1:c.828C>G	XP_011538671.1:p.Arg276=
XM_006718075.4:c.828C>G	XP_006718138.1:p.Arg276=
XM_011540369.2:c.828C>G	XP_011538671.1:p.Arg276=
NM_004273.5:c.828C>G MANE Select	NP_004264.2:p.Arg276=