Canonical Allele Identifier: CA1918977718
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009977G= , CM000672.2:g.72009977G= GRCh38
NC_000010.10:g.73769735G= , CM000672.1:g.73769735G= GRCh37
NC_000010.9:g.73439741G= NCBI36
NG_012635.1:g.50616G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1506G= MANE Select ENSP00000362207.4:n.*1506G=
ENST00000373115.4:c.*1506G= ENSP00000362207.4:n.*1506G=
NM_004273.4:c.*1506G= NP_004264.2:n.*1506G=
XM_006718075.2:c.*1506G= XP_006718138.1:n.*1506G=
XM_011540369.1:c.*1506G= XP_011538671.1:n.*1506G=
XM_006718075.4:c.*1506G= XP_006718138.1:n.*1506G=
XM_011540369.2:c.*1506G= XP_011538671.1:n.*1506G=
NM_004273.5:c.*1506G= MANE Select NP_004264.2:n.*1506G=
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