Canonical Allele Identifier: CA377146106
Gene: CHST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73767499T>A (hg19) chr10:g.72007741T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007741T>A , CM000672.2:g.72007741T>A GRCh38
NC_000010.10:g.73767499T>A , CM000672.1:g.73767499T>A GRCh37
NC_000010.9:g.73437505T>A NCBI36
NG_012635.1:g.48380T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.710T>A MANE Select ENSP00000362207.4:p.Phe237Tyr
ENST00000373115.4:c.710T>A ENSP00000362207.4:p.Phe237Tyr
NM_004273.4:c.710T>A NP_004264.2:p.Phe237Tyr
XM_006718075.2:c.710T>A XP_006718138.1:p.Phe237Tyr
XM_011540369.1:c.710T>A XP_011538671.1:p.Phe237Tyr
XM_006718075.4:c.710T>A XP_006718138.1:p.Phe237Tyr
XM_011540369.2:c.710T>A XP_011538671.1:p.Phe237Tyr
NM_004273.5:c.710T>A MANE Select NP_004264.2:p.Phe237Tyr
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