Canonical Allele Identifier: CA2324749807
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191702A= , CM000681.2:g.15191702A= GRCh38
NC_000019.9:g.15302513A= , CM000681.1:g.15302513A= GRCh37
NC_000019.8:g.15163513A= NCBI36
NG_009819.1:g.14280T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.802+43T= MANE Select ENSP00000263388.1:n.802+43T=
ENST00000263388.6:c.802+43T= ENSP00000263388.1:n.802+43T=
ENST00000601011.1:c.799+43T= ENSP00000473138.1:n.799+43T=
NM_000435.2:c.802+43T= NP_000426.2:n.802+43T=
XM_005259924.3:c.802+43T= XP_005259981.1:n.802+43T=
XM_005259924.4:c.802+43T= XP_005259981.1:n.802+43T=
NM_000435.3:c.802+43T= MANE Select NP_000426.2:n.802+43T=