Canonical Allele Identifier: CA2324747596
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187064C= , CM000681.2:g.15187064C= GRCh38
NC_000019.9:g.15297875C= , CM000681.1:g.15297875C= GRCh37
NC_000019.8:g.15158875C= NCBI36
NG_009819.1:g.18918G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1840+41G= MANE Select ENSP00000263388.1:n.1840+41G=
ENST00000263388.6:c.1840+41G= ENSP00000263388.1:n.1840+41G=
ENST00000601011.1:c.1837+41G= ENSP00000473138.1:n.1837+41G=
NM_000435.2:c.1840+41G= NP_000426.2:n.1840+41G=
XM_005259924.3:c.1840+41G= XP_005259981.1:n.1840+41G=
XM_005259924.4:c.1840+41G= XP_005259981.1:n.1840+41G=
NM_000435.3:c.1840+41G= MANE Select NP_000426.2:n.1840+41G=
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