Canonical Allele Identifier: CA2609587208
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009617G>T , CM000672.2:g.72009617G>T GRCh38
NC_000010.10:g.73769375G>T , CM000672.1:g.73769375G>T GRCh37
NC_000010.9:g.73439381G>T NCBI36
NG_012635.1:g.50256G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1146G>T MANE Select ENSP00000362207.4:n.*1146G>T
ENST00000373115.4:c.*1146G>T ENSP00000362207.4:n.*1146G>T
NM_004273.4:c.*1146G>T NP_004264.2:n.*1146G>T
XM_006718075.2:c.*1146G>T XP_006718138.1:n.*1146G>T
XM_011540369.1:c.*1146G>T XP_011538671.1:n.*1146G>T
XM_006718075.4:c.*1146G>T XP_006718138.1:n.*1146G>T
XM_011540369.2:c.*1146G>T XP_011538671.1:n.*1146G>T
NM_004273.5:c.*1146G>T MANE Select NP_004264.2:n.*1146G>T