Canonical Allele Identifier: CA1918976707
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008049C= , CM000672.2:g.72008049C= GRCh38
NC_000010.10:g.73767807C= , CM000672.1:g.73767807C= GRCh37
NC_000010.9:g.73437813C= NCBI36
NG_012635.1:g.48688C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1018C= MANE Select ENSP00000362207.4:p.Arg340=
ENST00000373115.4:c.1018C= ENSP00000362207.4:p.Arg340=
NM_004273.4:c.1018C= NP_004264.2:p.Arg340=
XM_006718075.2:c.1018C= XP_006718138.1:p.Arg340=
XM_011540369.1:c.1018C= XP_011538671.1:p.Arg340=
XM_006718075.4:c.1018C= XP_006718138.1:p.Arg340=
XM_011540369.2:c.1018C= XP_011538671.1:p.Arg340=
NM_004273.5:c.1018C= MANE Select NP_004264.2:p.Arg340=