Canonical Allele Identifier: CA2324747603
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187078T= , CM000681.2:g.15187078T= GRCh38
NC_000019.9:g.15297889T= , CM000681.1:g.15297889T= GRCh37
NC_000019.8:g.15158889T= NCBI36
NG_009819.1:g.18904A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1840+27A= MANE Select ENSP00000263388.1:n.1840+27A=
ENST00000263388.6:c.1840+27A= ENSP00000263388.1:n.1840+27A=
ENST00000601011.1:c.1837+27A= ENSP00000473138.1:n.1837+27A=
NM_000435.2:c.1840+27A= NP_000426.2:n.1840+27A=
XM_005259924.3:c.1840+27A= XP_005259981.1:n.1840+27A=
XM_005259924.4:c.1840+27A= XP_005259981.1:n.1840+27A=
NM_000435.3:c.1840+27A= MANE Select NP_000426.2:n.1840+27A=