Canonical Allele Identifier: CA10628910
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 300604
dbSNP Id: rs4148943

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009749C>T , CM000672.2:g.72009749C>T GRCh38
NC_000010.10:g.73769507C>T , CM000672.1:g.73769507C>T GRCh37
NC_000010.9:g.73439513C>T NCBI36
NG_012635.1:g.50388C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1278C>T MANE Select ENSP00000362207.4:n.*1278C>T
ENST00000373115.4:c.*1278C>T ENSP00000362207.4:n.*1278C>T
NM_004273.4:c.*1278C>T NP_004264.2:n.*1278C>T
XM_006718075.2:c.*1278C>T XP_006718138.1:n.*1278C>T
XM_011540369.1:c.*1278C>T XP_011538671.1:n.*1278C>T
XM_006718075.4:c.*1278C>T XP_006718138.1:n.*1278C>T
XM_011540369.2:c.*1278C>T XP_011538671.1:n.*1278C>T
NM_004273.5:c.*1278C>T MANE Select NP_004264.2:n.*1278C>T