Canonical Allele Identifier: CA1918977654
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009838T= , CM000672.2:g.72009838T= GRCh38
NC_000010.10:g.73769596T= , CM000672.1:g.73769596T= GRCh37
NC_000010.9:g.73439602T= NCBI36
NG_012635.1:g.50477T=

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1367T= MANE Select ENSP00000362207.4:n.*1367T=
ENST00000373115.4:c.*1367T= ENSP00000362207.4:n.*1367T=
NM_004273.4:c.*1367T= NP_004264.2:n.*1367T=
XM_006718075.2:c.*1367T= XP_006718138.1:n.*1367T=
XM_011540369.1:c.*1367T= XP_011538671.1:n.*1367T=
XM_006718075.4:c.*1367T= XP_006718138.1:n.*1367T=
XM_011540369.2:c.*1367T= XP_011538671.1:n.*1367T=
NM_004273.5:c.*1367T= MANE Select NP_004264.2:n.*1367T=
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