Canonical Allele Identifier: CA420189300
Gene: NOTCH2 HGNC NCBI

Linked Data

dbSNP Id: rs1379128384

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119915555C>T , CM000663.2:g.119915555C>T GRCh38
NC_000001.10:g.120458178C>T , CM000663.1:g.120458178C>T GRCh37
NC_000001.9:g.120259701C>T NCBI36
NG_008163.1:g.159099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256646.7:c.7167G>A MANE Select ENSP00000256646.2:p.Gln2389=
ENST00000256646.6:c.7167G>A ENSP00000256646.2:p.Gln2389=
NM_024408.3:c.7167G>A NP_077719.2:p.Gln2389=
XM_005270901.2:c.7050G>A XP_005270958.1:p.Gln2350=
XM_011541519.1:c.7155G>A XP_011539821.1:p.Gln2385=
XM_011541520.1:c.7050G>A XP_011539822.1:p.Gln2350=
NM_024408.4:c.7167G>A MANE Select NP_077719.2:p.Gln2389=