Canonical Allele Identifier: CA470284149

Gene: CHST3

Linked Data

• dbSNP Id: rs1026950461
• gnomAD v3: 10-72008012-C-T
• gnomAD v4: 10-72008012-C-T
• MyVariant Identifiers: chr10:g.73767770C>T (hg19) ; chr10:g.72008012C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008012C>T , CM000672.2:g.72008012C>T	GRCh38
NC_000010.10:g.73767770C>T , CM000672.1:g.73767770C>T	GRCh37
NC_000010.9:g.73437776C>T	NCBI36
NG_012635.1:g.48651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.981C>T MANE Select	ENSP00000362207.4:p.Asp327=
ENST00000373115.4:c.981C>T	ENSP00000362207.4:p.Asp327=
NM_004273.4:c.981C>T	NP_004264.2:p.Asp327=
XM_006718075.2:c.981C>T	XP_006718138.1:p.Asp327=
XM_011540369.1:c.981C>T	XP_011538671.1:p.Asp327=
XM_006718075.4:c.981C>T	XP_006718138.1:p.Asp327=
XM_011540369.2:c.981C>T	XP_011538671.1:p.Asp327=
NM_004273.5:c.981C>T MANE Select	NP_004264.2:p.Asp327=