Canonical Allele Identifier: CA2609587369
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009660-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009660C>A , CM000672.2:g.72009660C>A GRCh38
NC_000010.10:g.73769418C>A , CM000672.1:g.73769418C>A GRCh37
NC_000010.9:g.73439424C>A NCBI36
NG_012635.1:g.50299C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1189C>A MANE Select ENSP00000362207.4:n.*1189C>A
ENST00000373115.4:c.*1189C>A ENSP00000362207.4:n.*1189C>A
NM_004273.4:c.*1189C>A NP_004264.2:n.*1189C>A
XM_006718075.2:c.*1189C>A XP_006718138.1:n.*1189C>A
XM_011540369.1:c.*1189C>A XP_011538671.1:n.*1189C>A
XM_006718075.4:c.*1189C>A XP_006718138.1:n.*1189C>A
XM_011540369.2:c.*1189C>A XP_011538671.1:n.*1189C>A
NM_004273.5:c.*1189C>A MANE Select NP_004264.2:n.*1189C>A
Search 100 bp 5'
Search 100 bp 3'