Canonical Allele Identifier: CA2324749780
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191656G= , CM000681.2:g.15191656G= GRCh38
NC_000019.9:g.15302467G= , CM000681.1:g.15302467G= GRCh37
NC_000019.8:g.15163467G= NCBI36
NG_009819.1:g.14326C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.804C= MANE Select ENSP00000263388.1:p.Gly268=
ENST00000263388.6:c.804C= ENSP00000263388.1:p.Gly268=
ENST00000601011.1:c.801C= ENSP00000473138.1:p.Gly267=
NM_000435.2:c.804C= NP_000426.2:p.Gly268=
XM_005259924.3:c.804C= XP_005259981.1:p.Gly268=
XM_005259924.4:c.804C= XP_005259981.1:p.Gly268=
NM_000435.3:c.804C= MANE Select NP_000426.2:p.Gly268=