Canonical Allele Identifier: CA377151990
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2015793
ClinVar RCV Id: RCV002846535
gnomAD v4: 10-72008295-T-C
MyVariant Identifiers: chr10:g.73768053T>C (hg19) chr10:g.72008295T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008295T>C , CM000672.2:g.72008295T>C GRCh38
NC_000010.10:g.73768053T>C , CM000672.1:g.73768053T>C GRCh37
NC_000010.9:g.73438059T>C NCBI36
NG_012635.1:g.48934T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1264T>C MANE Select ENSP00000362207.4:p.Ser422Pro
ENST00000373115.4:c.1264T>C ENSP00000362207.4:p.Ser422Pro
NM_004273.4:c.1264T>C NP_004264.2:p.Ser422Pro
XM_006718075.2:c.1264T>C XP_006718138.1:p.Ser422Pro
XM_011540369.1:c.1264T>C XP_011538671.1:p.Ser422Pro
XM_006718075.4:c.1264T>C XP_006718138.1:p.Ser422Pro
XM_011540369.2:c.1264T>C XP_011538671.1:p.Ser422Pro
NM_004273.5:c.1264T>C MANE Select NP_004264.2:p.Ser422Pro
Search 100 bp 5'
Search 100 bp 3'