Canonical Allele Identifier: CA509816641
Gene: JAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10639351T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10658703T>C , CM000682.2:g.10658703T>C GRCh38
NC_000020.10:g.10639351T>C , CM000682.1:g.10639351T>C GRCh37
NC_000020.9:g.10587351T>C NCBI36
NG_007496.1:g.20344A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.459A>G MANE Select ENSP00000254958.4:p.Glu153=
ENST00000254958.9:c.459A>G ENSP00000254958.4:p.Glu153=
ENST00000423891.6:n.325A>G
NM_000214.2:c.459A>G NP_000205.1:p.Glu153=
NM_000214.3:c.459A>G MANE Select NP_000205.1:p.Glu153=
Search 100 bp 5'
Search 100 bp 3'