Canonical Allele Identifier: CA668113118
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs916903244

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009740C>T , CM000672.2:g.72009740C>T GRCh38
NC_000010.10:g.73769498C>T , CM000672.1:g.73769498C>T GRCh37
NC_000010.9:g.73439504C>T NCBI36
NG_012635.1:g.50379C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1269C>T MANE Select ENSP00000362207.4:n.*1269C>T
ENST00000373115.4:c.*1269C>T ENSP00000362207.4:n.*1269C>T
NM_004273.4:c.*1269C>T NP_004264.2:n.*1269C>T
XM_006718075.2:c.*1269C>T XP_006718138.1:n.*1269C>T
XM_011540369.1:c.*1269C>T XP_011538671.1:n.*1269C>T
XM_006718075.4:c.*1269C>T XP_006718138.1:n.*1269C>T
XM_011540369.2:c.*1269C>T XP_011538671.1:n.*1269C>T
NM_004273.5:c.*1269C>T MANE Select NP_004264.2:n.*1269C>T