Canonical Allele Identifier: CA470284645
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1362906854
gnomAD v2: 10-73767947-C-T
gnomAD v3: 10-72008189-C-T
gnomAD v4: 10-72008189-C-T
COSMIC: COSM4460255
MyVariant Identifiers: chr10:g.73767947C>T (hg19) chr10:g.72008189C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008189C>T , CM000672.2:g.72008189C>T GRCh38
NC_000010.10:g.73767947C>T , CM000672.1:g.73767947C>T GRCh37
NC_000010.9:g.73437953C>T NCBI36
NG_012635.1:g.48828C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1158C>T MANE Select ENSP00000362207.4:p.Tyr386=
ENST00000373115.4:c.1158C>T ENSP00000362207.4:p.Tyr386=
NM_004273.4:c.1158C>T NP_004264.2:p.Tyr386=
XM_006718075.2:c.1158C>T XP_006718138.1:p.Tyr386=
XM_011540369.1:c.1158C>T XP_011538671.1:p.Tyr386=
XM_006718075.4:c.1158C>T XP_006718138.1:p.Tyr386=
XM_011540369.2:c.1158C>T XP_011538671.1:p.Tyr386=
NM_004273.5:c.1158C>T MANE Select NP_004264.2:p.Tyr386=
Search 100 bp 5'
Search 100 bp 3'