Canonical Allele Identifier: CA209479745
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs544271000
gnomAD v2: 10-73769008-T-G
gnomAD v3: 10-72009250-T-G
gnomAD v4: 10-72009250-T-G
MyVariant Identifiers: chr10:g.73769008T>G (hg19) chr10:g.72009250T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009250T>G , CM000672.2:g.72009250T>G GRCh38
NC_000010.10:g.73769008T>G , CM000672.1:g.73769008T>G GRCh37
NC_000010.9:g.73439014T>G NCBI36
NG_012635.1:g.49889T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*779T>G MANE Select ENSP00000362207.4:n.*779T>G
ENST00000373115.4:c.*779T>G ENSP00000362207.4:n.*779T>G
NM_004273.4:c.*779T>G NP_004264.2:n.*779T>G
XM_006718075.2:c.*779T>G XP_006718138.1:n.*779T>G
XM_011540369.1:c.*779T>G XP_011538671.1:n.*779T>G
XM_006718075.4:c.*779T>G XP_006718138.1:n.*779T>G
XM_011540369.2:c.*779T>G XP_011538671.1:n.*779T>G
NM_004273.5:c.*779T>G MANE Select NP_004264.2:n.*779T>G
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