Canonical Allele Identifier: CA377151886
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008280A>T , CM000672.2:g.72008280A>T GRCh38
NC_000010.10:g.73768038A>T , CM000672.1:g.73768038A>T GRCh37
NC_000010.9:g.73438044A>T NCBI36
NG_012635.1:g.48919A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1249A>T MANE Select ENSP00000362207.4:p.Thr417Ser
ENST00000373115.4:c.1249A>T ENSP00000362207.4:p.Thr417Ser
NM_004273.4:c.1249A>T NP_004264.2:p.Thr417Ser
XM_006718075.2:c.1249A>T XP_006718138.1:p.Thr417Ser
XM_011540369.1:c.1249A>T XP_011538671.1:p.Thr417Ser
XM_006718075.4:c.1249A>T XP_006718138.1:p.Thr417Ser
XM_011540369.2:c.1249A>T XP_011538671.1:p.Thr417Ser
NM_004273.5:c.1249A>T MANE Select NP_004264.2:p.Thr417Ser