Canonical Allele Identifier: CA2324749824
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191739G= , CM000681.2:g.15191739G= GRCh38
NC_000019.9:g.15302550G= , CM000681.1:g.15302550G= GRCh37
NC_000019.8:g.15163550G= NCBI36
NG_009819.1:g.14243C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.802+6C= MANE Select ENSP00000263388.1:n.802+6C=
ENST00000263388.6:c.802+6C= ENSP00000263388.1:n.802+6C=
ENST00000601011.1:c.799+6C= ENSP00000473138.1:n.799+6C=
NM_000435.2:c.802+6C= NP_000426.2:n.802+6C=
XM_005259924.3:c.802+6C= XP_005259981.1:n.802+6C=
XM_005259924.4:c.802+6C= XP_005259981.1:n.802+6C=
NM_000435.3:c.802+6C= MANE Select NP_000426.2:n.802+6C=