Canonical Allele Identifier: CA1918977601
Gene: CHST3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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