Canonical Allele Identifier: CA2324744465
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180632T= , CM000681.2:g.15180632T= GRCh38
NC_000019.9:g.15291443T= , CM000681.1:g.15291443T= GRCh37
NC_000019.8:g.15152443T= NCBI36
NG_009819.1:g.25350A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3142+49A= MANE Select ENSP00000263388.1:n.3142+49A=
ENST00000263388.6:c.3142+49A= ENSP00000263388.1:n.3142+49A=
ENST00000601011.1:c.2983+49A= ENSP00000473138.1:n.2983+49A=
NM_000435.2:c.3142+49A= NP_000426.2:n.3142+49A=
XM_005259924.3:c.2986+49A= XP_005259981.1:n.2986+49A=
XM_005259924.4:c.2986+49A= XP_005259981.1:n.2986+49A=
NM_000435.3:c.3142+49A= MANE Select NP_000426.2:n.3142+49A=
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