Canonical Allele Identifier: CA5548226
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs771208378

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008292T>A , CM000672.2:g.72008292T>A GRCh38
NC_000010.10:g.73768050T>A , CM000672.1:g.73768050T>A GRCh37
NC_000010.9:g.73438056T>A NCBI36
NG_012635.1:g.48931T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1261T>A MANE Select ENSP00000362207.4:p.Ser421Thr
ENST00000373115.4:c.1261T>A ENSP00000362207.4:p.Ser421Thr
NM_004273.4:c.1261T>A NP_004264.2:p.Ser421Thr
XM_006718075.2:c.1261T>A XP_006718138.1:p.Ser421Thr
XM_011540369.1:c.1261T>A XP_011538671.1:p.Ser421Thr
XM_006718075.4:c.1261T>A XP_006718138.1:p.Ser421Thr
XM_011540369.2:c.1261T>A XP_011538671.1:p.Ser421Thr
NM_004273.5:c.1261T>A MANE Select NP_004264.2:p.Ser421Thr