Canonical Allele Identifier: CA2324747802
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187432C= , CM000681.2:g.15187432C= GRCh38
NC_000019.9:g.15298243C= , CM000681.1:g.15298243C= GRCh37
NC_000019.8:g.15159243C= NCBI36
NG_009819.1:g.18550G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-94G= MANE Select ENSP00000263388.1:n.1607-94G=
ENST00000263388.6:c.1607-94G= ENSP00000263388.1:n.1607-94G=
ENST00000601011.1:c.1604-94G= ENSP00000473138.1:n.1604-94G=
NM_000435.2:c.1607-94G= NP_000426.2:n.1607-94G=
XM_005259924.3:c.1607-94G= XP_005259981.1:n.1607-94G=
XM_005259924.4:c.1607-94G= XP_005259981.1:n.1607-94G=
NM_000435.3:c.1607-94G= MANE Select NP_000426.2:n.1607-94G=
Search 100 bp 5'
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