Canonical Allele Identifier: CA668112869

Gene: CHST3

Linked Data

• dbSNP Id: rs1406036629
• MyVariant Identifiers: chr10:g.73769215C>A (hg19) ; chr10:g.72009457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009457C>A , CM000672.2:g.72009457C>A	GRCh38
NC_000010.10:g.73769215C>A , CM000672.1:g.73769215C>A	GRCh37
NC_000010.9:g.73439221C>A	NCBI36
NG_012635.1:g.50096C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*986C>A MANE Select	ENSP00000362207.4:n.*986C>A
ENST00000373115.4:c.*986C>A	ENSP00000362207.4:n.*986C>A
NM_004273.4:c.*986C>A	NP_004264.2:n.*986C>A
XM_006718075.2:c.*986C>A	XP_006718138.1:n.*986C>A
XM_011540369.1:c.*986C>A	XP_011538671.1:n.*986C>A
XM_006718075.4:c.*986C>A	XP_006718138.1:n.*986C>A
XM_011540369.2:c.*986C>A	XP_011538671.1:n.*986C>A
NM_004273.5:c.*986C>A MANE Select	NP_004264.2:n.*986C>A