Canonical Allele Identifier: CA2324750032
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192182G= , CM000681.2:g.15192182G= GRCh38
NC_000019.9:g.15302993G= , CM000681.1:g.15302993G= GRCh37
NC_000019.8:g.15163993G= NCBI36
NG_009819.1:g.13800C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.457C= MANE Select ENSP00000263388.1:p.Arg153=
ENST00000263388.6:c.457C= ENSP00000263388.1:p.Arg153=
ENST00000601011.1:c.454C= ENSP00000473138.1:p.Arg152=
NM_000435.2:c.457C= NP_000426.2:p.Arg153=
XM_005259924.3:c.457C= XP_005259981.1:p.Arg153=
XM_005259924.4:c.457C= XP_005259981.1:p.Arg153=
NM_000435.3:c.457C= MANE Select NP_000426.2:p.Arg153=