Canonical Allele Identifier: CA2324746230
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184245A= , CM000681.2:g.15184245A= GRCh38
NC_000019.9:g.15295056A= , CM000681.1:g.15295056A= GRCh37
NC_000019.8:g.15156056A= NCBI36
NG_009819.1:g.21737T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.2566+50T= MANE Select ENSP00000263388.1:n.2566+50T=
ENST00000263388.6:c.2566+50T= ENSP00000263388.1:n.2566+50T=
ENST00000601011.1:c.2407+661T= ENSP00000473138.1:n.2407+661T=
NM_000435.2:c.2566+50T= NP_000426.2:n.2566+50T=
XM_005259924.3:c.2410+661T= XP_005259981.1:n.2410+661T=
XM_005259924.4:c.2410+661T= XP_005259981.1:n.2410+661T=
NM_000435.3:c.2566+50T= MANE Select NP_000426.2:n.2566+50T=
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