Canonical Allele Identifier: CA509661747
Gene: JAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10630989A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10650341A>T , CM000682.2:g.10650341A>T GRCh38
NC_000020.10:g.10630989A>T , CM000682.1:g.10630989A>T GRCh37
NC_000020.9:g.10578989A>T NCBI36
NG_007496.1:g.28706T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000254958.10:c.1140T>A MANE Select ENSP00000254958.4:p.Pro380=
ENST00000617965.2:n.1729T>A
ENST00000254958.9:c.1140T>A ENSP00000254958.4:p.Pro380=
ENST00000423891.6:n.1006T>A
NM_000214.2:c.1140T>A NP_000205.1:p.Pro380=
NM_000214.3:c.1140T>A MANE Select NP_000205.1:p.Pro380=
Search 100 bp 5'
Search 100 bp 3'