Canonical Allele Identifier: CA2324747793
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187416T= , CM000681.2:g.15187416T= GRCh38
NC_000019.9:g.15298227T= , CM000681.1:g.15298227T= GRCh37
NC_000019.8:g.15159227T= NCBI36
NG_009819.1:g.18566A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-78A= MANE Select ENSP00000263388.1:n.1607-78A=
ENST00000263388.6:c.1607-78A= ENSP00000263388.1:n.1607-78A=
ENST00000601011.1:c.1604-78A= ENSP00000473138.1:n.1604-78A=
NM_000435.2:c.1607-78A= NP_000426.2:n.1607-78A=
XM_005259924.3:c.1607-78A= XP_005259981.1:n.1607-78A=
XM_005259924.4:c.1607-78A= XP_005259981.1:n.1607-78A=
NM_000435.3:c.1607-78A= MANE Select NP_000426.2:n.1607-78A=
Search 100 bp 5'
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