Canonical Allele Identifier: CA470284004
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1240581479
gnomAD v2: 10-73768019-C-T
gnomAD v3: 10-72008261-C-T
gnomAD v4: 10-72008261-C-T
COSMIC: COSM5999283
MyVariant Identifiers: chr10:g.73768019C>T (hg19) chr10:g.72008261C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008261C>T , CM000672.2:g.72008261C>T GRCh38
NC_000010.10:g.73768019C>T , CM000672.1:g.73768019C>T GRCh37
NC_000010.9:g.73438025C>T NCBI36
NG_012635.1:g.48900C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1230C>T MANE Select ENSP00000362207.4:p.Asp410=
ENST00000373115.4:c.1230C>T ENSP00000362207.4:p.Asp410=
NM_004273.4:c.1230C>T NP_004264.2:p.Asp410=
XM_006718075.2:c.1230C>T XP_006718138.1:p.Asp410=
XM_011540369.1:c.1230C>T XP_011538671.1:p.Asp410=
XM_006718075.4:c.1230C>T XP_006718138.1:p.Asp410=
XM_011540369.2:c.1230C>T XP_011538671.1:p.Asp410=
NM_004273.5:c.1230C>T MANE Select NP_004264.2:p.Asp410=
Search 100 bp 5'
Search 100 bp 3'