Canonical Allele Identifier: CA2324747532
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186934C= , CM000681.2:g.15186934C= GRCh38
NC_000019.9:g.15297745C= , CM000681.1:g.15297745C= GRCh37
NC_000019.8:g.15158745C= NCBI36
NG_009819.1:g.19048G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1895G= MANE Select ENSP00000263388.1:p.Gly632=
ENST00000263388.6:c.1895G= ENSP00000263388.1:p.Gly632=
ENST00000601011.1:c.1892G= ENSP00000473138.1:p.Gly631=
NM_000435.2:c.1895G= NP_000426.2:p.Gly632=
XM_005259924.3:c.1895G= XP_005259981.1:p.Gly632=
XM_005259924.4:c.1895G= XP_005259981.1:p.Gly632=
NM_000435.3:c.1895G= MANE Select NP_000426.2:p.Gly632=