Canonical Allele Identifier: CA2609587629
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009739-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009739T>G , CM000672.2:g.72009739T>G GRCh38
NC_000010.10:g.73769497T>G , CM000672.1:g.73769497T>G GRCh37
NC_000010.9:g.73439503T>G NCBI36
NG_012635.1:g.50378T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1268T>G MANE Select ENSP00000362207.4:n.*1268T>G
ENST00000373115.4:c.*1268T>G ENSP00000362207.4:n.*1268T>G
NM_004273.4:c.*1268T>G NP_004264.2:n.*1268T>G
XM_006718075.2:c.*1268T>G XP_006718138.1:n.*1268T>G
XM_011540369.1:c.*1268T>G XP_011538671.1:n.*1268T>G
XM_006718075.4:c.*1268T>G XP_006718138.1:n.*1268T>G
XM_011540369.2:c.*1268T>G XP_011538671.1:n.*1268T>G
NM_004273.5:c.*1268T>G MANE Select NP_004264.2:n.*1268T>G
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