Canonical Allele Identifier: CA929816873

Gene: CHST3

Linked Data

• dbSNP Id: rs1840087936
• gnomAD v3: 10-72009650-C-T
• gnomAD v4: 10-72009650-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009650C>T , CM000672.2:g.72009650C>T	GRCh38
NC_000010.10:g.73769408C>T , CM000672.1:g.73769408C>T	GRCh37
NC_000010.9:g.73439414C>T	NCBI36
NG_012635.1:g.50289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1179C>T MANE Select	ENSP00000362207.4:n.*1179C>T
ENST00000373115.4:c.*1179C>T	ENSP00000362207.4:n.*1179C>T
NM_004273.4:c.*1179C>T	NP_004264.2:n.*1179C>T
XM_006718075.2:c.*1179C>T	XP_006718138.1:n.*1179C>T
XM_011540369.1:c.*1179C>T	XP_011538671.1:n.*1179C>T
XM_006718075.4:c.*1179C>T	XP_006718138.1:n.*1179C>T
XM_011540369.2:c.*1179C>T	XP_011538671.1:n.*1179C>T
NM_004273.5:c.*1179C>T MANE Select	NP_004264.2:n.*1179C>T