Canonical Allele Identifier: CA209479320
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1034905438
MyVariant Identifiers: chr10:g.73767781A>C (hg19) chr10:g.72008023A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008023A>C , CM000672.2:g.72008023A>C GRCh38
NC_000010.10:g.73767781A>C , CM000672.1:g.73767781A>C GRCh37
NC_000010.9:g.73437787A>C NCBI36
NG_012635.1:g.48662A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.992A>C MANE Select ENSP00000362207.4:p.Asp331Ala
ENST00000373115.4:c.992A>C ENSP00000362207.4:p.Asp331Ala
NM_004273.4:c.992A>C NP_004264.2:p.Asp331Ala
XM_006718075.2:c.992A>C XP_006718138.1:p.Asp331Ala
XM_011540369.1:c.992A>C XP_011538671.1:p.Asp331Ala
XM_006718075.4:c.992A>C XP_006718138.1:p.Asp331Ala
XM_011540369.2:c.992A>C XP_011538671.1:p.Asp331Ala
NM_004273.5:c.992A>C MANE Select NP_004264.2:p.Asp331Ala
Search 100 bp 5'
Search 100 bp 3'