Canonical Allele Identifier: CA1918977340
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009239C= , CM000672.2:g.72009239C= GRCh38
NC_000010.10:g.73768997C= , CM000672.1:g.73768997C= GRCh37
NC_000010.9:g.73439003C= NCBI36
NG_012635.1:g.49878C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*768C= MANE Select ENSP00000362207.4:n.*768C=
ENST00000373115.4:c.*768C= ENSP00000362207.4:n.*768C=
NM_004273.4:c.*768C= NP_004264.2:n.*768C=
XM_006718075.2:c.*768C= XP_006718138.1:n.*768C=
XM_011540369.1:c.*768C= XP_011538671.1:n.*768C=
XM_006718075.4:c.*768C= XP_006718138.1:n.*768C=
XM_011540369.2:c.*768C= XP_011538671.1:n.*768C=
NM_004273.5:c.*768C= MANE Select NP_004264.2:n.*768C=