Canonical Allele Identifier: CA668113057

Gene: CHST3

Linked Data

• dbSNP Id: rs1324797545
• gnomAD v3: 10-72009653-C-T
• gnomAD v4: 10-72009653-C-T
• MyVariant Identifiers: chr10:g.73769411C>T (hg19) ; chr10:g.72009653C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009653C>T , CM000672.2:g.72009653C>T	GRCh38
NC_000010.10:g.73769411C>T , CM000672.1:g.73769411C>T	GRCh37
NC_000010.9:g.73439417C>T	NCBI36
NG_012635.1:g.50292C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373115.5:c.*1182C>T MANE Select	ENSP00000362207.4:n.*1182C>T
ENST00000373115.4:c.*1182C>T	ENSP00000362207.4:n.*1182C>T
NM_004273.4:c.*1182C>T	NP_004264.2:n.*1182C>T
XM_006718075.2:c.*1182C>T	XP_006718138.1:n.*1182C>T
XM_011540369.1:c.*1182C>T	XP_011538671.1:n.*1182C>T
XM_006718075.4:c.*1182C>T	XP_006718138.1:n.*1182C>T
XM_011540369.2:c.*1182C>T	XP_011538671.1:n.*1182C>T
NM_004273.5:c.*1182C>T MANE Select	NP_004264.2:n.*1182C>T