Canonical Allele Identifier: CA2324747841
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187493T= , CM000681.2:g.15187493T= GRCh38
NC_000019.9:g.15298304T= , CM000681.1:g.15298304T= GRCh37
NC_000019.8:g.15159304T= NCBI36
NG_009819.1:g.18489A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-155A= MANE Select ENSP00000263388.1:n.1607-155A=
ENST00000263388.6:c.1607-155A= ENSP00000263388.1:n.1607-155A=
ENST00000601011.1:c.1604-155A= ENSP00000473138.1:n.1604-155A=
NM_000435.2:c.1607-155A= NP_000426.2:n.1607-155A=
XM_005259924.3:c.1607-155A= XP_005259981.1:n.1607-155A=
XM_005259924.4:c.1607-155A= XP_005259981.1:n.1607-155A=
NM_000435.3:c.1607-155A= MANE Select NP_000426.2:n.1607-155A=