Canonical Allele Identifier: CA470283906
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2889669
ClinVar RCV Id: RCV003633390
dbSNP Id: rs1840060033
gnomAD v3: 10-72007826-C-G
gnomAD v4: 10-72007826-C-G
MyVariant Identifiers: chr10:g.73767584C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007826C>G , CM000672.2:g.72007826C>G GRCh38
NC_000010.10:g.73767584C>G , CM000672.1:g.73767584C>G GRCh37
NC_000010.9:g.73437590C>G NCBI36
NG_012635.1:g.48465C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.795C>G MANE Select ENSP00000362207.4:p.Arg265=
ENST00000373115.4:c.795C>G ENSP00000362207.4:p.Arg265=
NM_004273.4:c.795C>G NP_004264.2:p.Arg265=
XM_006718075.2:c.795C>G XP_006718138.1:p.Arg265=
XM_011540369.1:c.795C>G XP_011538671.1:p.Arg265=
XM_006718075.4:c.795C>G XP_006718138.1:p.Arg265=
XM_011540369.2:c.795C>G XP_011538671.1:p.Arg265=
NM_004273.5:c.795C>G MANE Select NP_004264.2:p.Arg265=
Search 100 bp 5'
Search 100 bp 3'