Canonical Allele Identifier: CA594328327
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs933667281
gnomAD v2: 10-73769625-G-C
gnomAD v3: 10-72009867-G-C
gnomAD v4: 10-72009867-G-C
MyVariant Identifiers: chr10:g.73769625G>C (hg19) chr10:g.72009867G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009867G>C , CM000672.2:g.72009867G>C GRCh38
NC_000010.10:g.73769625G>C , CM000672.1:g.73769625G>C GRCh37
NC_000010.9:g.73439631G>C NCBI36
NG_012635.1:g.50506G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1396G>C MANE Select ENSP00000362207.4:n.*1396G>C
ENST00000373115.4:c.*1396G>C ENSP00000362207.4:n.*1396G>C
NM_004273.4:c.*1396G>C NP_004264.2:n.*1396G>C
XM_006718075.2:c.*1396G>C XP_006718138.1:n.*1396G>C
XM_011540369.1:c.*1396G>C XP_011538671.1:n.*1396G>C
XM_006718075.4:c.*1396G>C XP_006718138.1:n.*1396G>C
XM_011540369.2:c.*1396G>C XP_011538671.1:n.*1396G>C
NM_004273.5:c.*1396G>C MANE Select NP_004264.2:n.*1396G>C
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