Canonical Allele Identifier: CA2609587381
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009664A>T , CM000672.2:g.72009664A>T GRCh38
NC_000010.10:g.73769422A>T , CM000672.1:g.73769422A>T GRCh37
NC_000010.9:g.73439428A>T NCBI36
NG_012635.1:g.50303A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1193A>T MANE Select ENSP00000362207.4:n.*1193A>T
ENST00000373115.4:c.*1193A>T ENSP00000362207.4:n.*1193A>T
NM_004273.4:c.*1193A>T NP_004264.2:n.*1193A>T
XM_006718075.2:c.*1193A>T XP_006718138.1:n.*1193A>T
XM_011540369.1:c.*1193A>T XP_011538671.1:n.*1193A>T
XM_006718075.4:c.*1193A>T XP_006718138.1:n.*1193A>T
XM_011540369.2:c.*1193A>T XP_011538671.1:n.*1193A>T
NM_004273.5:c.*1193A>T MANE Select NP_004264.2:n.*1193A>T