Canonical Allele Identifier: CA509816463
Gene: JAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10639231G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10658583G>T , CM000682.2:g.10658583G>T GRCh38
NC_000020.10:g.10639231G>T , CM000682.1:g.10639231G>T GRCh37
NC_000020.9:g.10587231G>T NCBI36
NG_007496.1:g.20464C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.579C>A MANE Select ENSP00000254958.4:p.Gly193=
ENST00000254958.9:c.579C>A ENSP00000254958.4:p.Gly193=
ENST00000423891.6:n.445C>A
NM_000214.2:c.579C>A NP_000205.1:p.Gly193=
NM_000214.3:c.579C>A MANE Select NP_000205.1:p.Gly193=
Search 100 bp 5'
Search 100 bp 3'