Canonical Allele Identifier: CA2324747586
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187039T= , CM000681.2:g.15187039T= GRCh38
NC_000019.9:g.15297850T= , CM000681.1:g.15297850T= GRCh37
NC_000019.8:g.15158850T= NCBI36
NG_009819.1:g.18943A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.1841-51A= MANE Select ENSP00000263388.1:n.1841-51A=
ENST00000263388.6:c.1841-51A= ENSP00000263388.1:n.1841-51A=
ENST00000601011.1:c.1838-51A= ENSP00000473138.1:n.1838-51A=
NM_000435.2:c.1841-51A= NP_000426.2:n.1841-51A=
XM_005259924.3:c.1841-51A= XP_005259981.1:n.1841-51A=
XM_005259924.4:c.1841-51A= XP_005259981.1:n.1841-51A=
NM_000435.3:c.1841-51A= MANE Select NP_000426.2:n.1841-51A=