Canonical Allele Identifier: CA209479977
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1020253797
MyVariant Identifiers: chr10:g.72010032G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72010032G>C , CM000672.2:g.72010032G>C GRCh38
NC_000010.10:g.73769790G>C , CM000672.1:g.73769790G>C GRCh37
NC_000010.9:g.73439796G>C NCBI36
NG_012635.1:g.50671G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1561G>C MANE Select ENSP00000362207.4:n.*1561G>C
ENST00000373115.4:c.*1561G>C ENSP00000362207.4:n.*1561G>C
NM_004273.4:c.*1561G>C NP_004264.2:n.*1561G>C
XM_006718075.2:c.*1561G>C XP_006718138.1:n.*1561G>C
XM_011540369.1:c.*1561G>C XP_011538671.1:n.*1561G>C
XM_006718075.4:c.*1561G>C XP_006718138.1:n.*1561G>C
XM_011540369.2:c.*1561G>C XP_011538671.1:n.*1561G>C
NM_004273.5:c.*1561G>C MANE Select NP_004264.2:n.*1561G>C
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