Canonical Allele Identifier: CA668113088
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs756598951
gnomAD v3: 10-72009671-C-A
gnomAD v4: 10-72009671-C-A
MyVariant Identifiers: chr10:g.73769429C>A (hg19) chr10:g.72009671C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009671C>A , CM000672.2:g.72009671C>A GRCh38
NC_000010.10:g.73769429C>A , CM000672.1:g.73769429C>A GRCh37
NC_000010.9:g.73439435C>A NCBI36
NG_012635.1:g.50310C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1200C>A MANE Select ENSP00000362207.4:n.*1200C>A
ENST00000373115.4:c.*1200C>A ENSP00000362207.4:n.*1200C>A
NM_004273.4:c.*1200C>A NP_004264.2:n.*1200C>A
XM_006718075.2:c.*1200C>A XP_006718138.1:n.*1200C>A
XM_011540369.1:c.*1200C>A XP_011538671.1:n.*1200C>A
XM_006718075.4:c.*1200C>A XP_006718138.1:n.*1200C>A
XM_011540369.2:c.*1200C>A XP_011538671.1:n.*1200C>A
NM_004273.5:c.*1200C>A MANE Select NP_004264.2:n.*1200C>A
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