Canonical Allele Identifier: CA9764622
Gene: JAG1 HGNC NCBI

Linked Data

dbSNP Id: rs377620636

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10645263G>A , CM000682.2:g.10645263G>A GRCh38
NC_000020.10:g.10625911G>A , CM000682.1:g.10625911G>A GRCh37
NC_000020.9:g.10573911G>A NCBI36
NG_007496.1:g.33784C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.2114-7C>T MANE Select ENSP00000254958.4:n.2114-7C>T
ENST00000617965.2:n.2703-7C>T
ENST00000254958.9:c.2114-7C>T ENSP00000254958.4:n.2114-7C>T
ENST00000423891.6:n.1980-7C>T
ENST00000488480.2:n.511-7C>T
NM_000214.2:c.2114-7C>T NP_000205.1:n.2114-7C>T
NM_000214.3:c.2114-7C>T MANE Select NP_000205.1:n.2114-7C>T