Canonical Allele Identifier: CA2324746282
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184340A= , CM000681.2:g.15184340A= GRCh38
NC_000019.9:g.15295151A= , CM000681.1:g.15295151A= GRCh37
NC_000019.8:g.15156151A= NCBI36
NG_009819.1:g.21642T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.2521T= MANE Select ENSP00000263388.1:p.Tyr841=
ENST00000263388.6:c.2521T= ENSP00000263388.1:p.Tyr841=
ENST00000601011.1:c.2407+566T= ENSP00000473138.1:n.2407+566T=
NM_000435.2:c.2521T= NP_000426.2:p.Tyr841=
XM_005259924.3:c.2410+566T= XP_005259981.1:n.2410+566T=
XM_005259924.4:c.2410+566T= XP_005259981.1:n.2410+566T=
NM_000435.3:c.2521T= MANE Select NP_000426.2:p.Tyr841=