Canonical Allele Identifier: CA2324746263
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184295T= , CM000681.2:g.15184295T= GRCh38
NC_000019.9:g.15295106T= , CM000681.1:g.15295106T= GRCh37
NC_000019.8:g.15156106T= NCBI36
NG_009819.1:g.21687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.2566A= MANE Select ENSP00000263388.1:p.Asn856=
ENST00000263388.6:c.2566A= ENSP00000263388.1:p.Asn856=
ENST00000601011.1:c.2407+611A= ENSP00000473138.1:n.2407+611A=
NM_000435.2:c.2566A= NP_000426.2:p.Asn856=
XM_005259924.3:c.2410+611A= XP_005259981.1:n.2410+611A=
XM_005259924.4:c.2410+611A= XP_005259981.1:n.2410+611A=
NM_000435.3:c.2566A= MANE Select NP_000426.2:p.Asn856=