Canonical Allele Identifier: CA2609586620
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009220-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009220C>A , CM000672.2:g.72009220C>A GRCh38
NC_000010.10:g.73768978C>A , CM000672.1:g.73768978C>A GRCh37
NC_000010.9:g.73438984C>A NCBI36
NG_012635.1:g.49859C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*749C>A MANE Select ENSP00000362207.4:n.*749C>A
ENST00000373115.4:c.*749C>A ENSP00000362207.4:n.*749C>A
NM_004273.4:c.*749C>A NP_004264.2:n.*749C>A
XM_006718075.2:c.*749C>A XP_006718138.1:n.*749C>A
XM_011540369.1:c.*749C>A XP_011538671.1:n.*749C>A
XM_006718075.4:c.*749C>A XP_006718138.1:n.*749C>A
XM_011540369.2:c.*749C>A XP_011538671.1:n.*749C>A
NM_004273.5:c.*749C>A MANE Select NP_004264.2:n.*749C>A
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