Canonical Allele Identifier: CA2324747813
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187459A= , CM000681.2:g.15187459A= GRCh38
NC_000019.9:g.15298270A= , CM000681.1:g.15298270A= GRCh37
NC_000019.8:g.15159270A= NCBI36
NG_009819.1:g.18523T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-121T= MANE Select ENSP00000263388.1:n.1607-121T=
ENST00000263388.6:c.1607-121T= ENSP00000263388.1:n.1607-121T=
ENST00000601011.1:c.1604-121T= ENSP00000473138.1:n.1604-121T=
NM_000435.2:c.1607-121T= NP_000426.2:n.1607-121T=
XM_005259924.3:c.1607-121T= XP_005259981.1:n.1607-121T=
XM_005259924.4:c.1607-121T= XP_005259981.1:n.1607-121T=
NM_000435.3:c.1607-121T= MANE Select NP_000426.2:n.1607-121T=