Canonical Allele Identifier: CA2324744432
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180571A= , CM000681.2:g.15180571A= GRCh38
NC_000019.9:g.15291382A= , CM000681.1:g.15291382A= GRCh37
NC_000019.8:g.15152382A= NCBI36
NG_009819.1:g.25411T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3142+110T= MANE Select ENSP00000263388.1:n.3142+110T=
ENST00000263388.6:c.3142+110T= ENSP00000263388.1:n.3142+110T=
ENST00000601011.1:c.2983+110T= ENSP00000473138.1:n.2983+110T=
NM_000435.2:c.3142+110T= NP_000426.2:n.3142+110T=
XM_005259924.3:c.2986+110T= XP_005259981.1:n.2986+110T=
XM_005259924.4:c.2986+110T= XP_005259981.1:n.2986+110T=
NM_000435.3:c.3142+110T= MANE Select NP_000426.2:n.3142+110T=
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