Canonical Allele Identifier: CA929816674

Gene: CHST3

Linked Data

• dbSNP Id: rs1766347420
• gnomAD v3: 10-72009444-G-T
• gnomAD v4: 10-72009444-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009444G>T , CM000672.2:g.72009444G>T	GRCh38
NC_000010.10:g.73769202G>T , CM000672.1:g.73769202G>T	GRCh37
NC_000010.9:g.73439208G>T	NCBI36
NG_012635.1:g.50083G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*973G>T MANE Select	ENSP00000362207.4:n.*973G>T
ENST00000373115.4:c.*973G>T	ENSP00000362207.4:n.*973G>T
NM_004273.4:c.*973G>T	NP_004264.2:n.*973G>T
XM_006718075.2:c.*973G>T	XP_006718138.1:n.*973G>T
XM_011540369.1:c.*973G>T	XP_011538671.1:n.*973G>T
XM_006718075.4:c.*973G>T	XP_006718138.1:n.*973G>T
XM_011540369.2:c.*973G>T	XP_011538671.1:n.*973G>T
NM_004273.5:c.*973G>T MANE Select	NP_004264.2:n.*973G>T