Canonical Allele Identifier: CA2324747528
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186926G= , CM000681.2:g.15186926G= GRCh38
NC_000019.9:g.15297737G= , CM000681.1:g.15297737G= GRCh37
NC_000019.8:g.15158737G= NCBI36
NG_009819.1:g.19056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1903C= MANE Select ENSP00000263388.1:p.Arg635=
ENST00000263388.6:c.1903C= ENSP00000263388.1:p.Arg635=
ENST00000601011.1:c.1900C= ENSP00000473138.1:p.Arg634=
NM_000435.2:c.1903C= NP_000426.2:p.Arg635=
XM_005259924.3:c.1903C= XP_005259981.1:p.Arg635=
XM_005259924.4:c.1903C= XP_005259981.1:p.Arg635=
NM_000435.3:c.1903C= MANE Select NP_000426.2:p.Arg635=