Canonical Allele Identifier: CA5548163
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs757896210
ExAC: 10:73767556 A / C
gnomAD v2: 10-73767556-A-C
gnomAD v4: 10-72007798-A-C
MyVariant Identifiers: chr10:g.73767556A>C (hg19) chr10:g.72007798A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007798A>C , CM000672.2:g.72007798A>C GRCh38
NC_000010.10:g.73767556A>C , CM000672.1:g.73767556A>C GRCh37
NC_000010.9:g.73437562A>C NCBI36
NG_012635.1:g.48437A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.767A>C MANE Select ENSP00000362207.4:p.Asn256Thr
ENST00000373115.4:c.767A>C ENSP00000362207.4:p.Asn256Thr
NM_004273.4:c.767A>C NP_004264.2:p.Asn256Thr
XM_006718075.2:c.767A>C XP_006718138.1:p.Asn256Thr
XM_011540369.1:c.767A>C XP_011538671.1:p.Asn256Thr
XM_006718075.4:c.767A>C XP_006718138.1:p.Asn256Thr
XM_011540369.2:c.767A>C XP_011538671.1:p.Asn256Thr
NM_004273.5:c.767A>C MANE Select NP_004264.2:p.Asn256Thr
Search 100 bp 5'
Search 100 bp 3'