Canonical Allele Identifier: CA2324747530
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186929A= , CM000681.2:g.15186929A= GRCh38
NC_000019.9:g.15297740A= , CM000681.1:g.15297740A= GRCh37
NC_000019.8:g.15158740A= NCBI36
NG_009819.1:g.19053T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1900T= MANE Select ENSP00000263388.1:p.Cys634=
ENST00000263388.6:c.1900T= ENSP00000263388.1:p.Cys634=
ENST00000601011.1:c.1897T= ENSP00000473138.1:p.Cys633=
NM_000435.2:c.1900T= NP_000426.2:p.Cys634=
XM_005259924.3:c.1900T= XP_005259981.1:p.Cys634=
XM_005259924.4:c.1900T= XP_005259981.1:p.Cys634=
NM_000435.3:c.1900T= MANE Select NP_000426.2:p.Cys634=