Canonical Allele Identifier: CA9263882
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs779932875

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192184C>T , CM000681.2:g.15192184C>T GRCh38
NC_000019.9:g.15302995C>T , CM000681.1:g.15302995C>T GRCh37
NC_000019.8:g.15163995C>T NCBI36
NG_009819.1:g.13798G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.455G>A MANE Select ENSP00000263388.1:p.Gly152Asp
ENST00000263388.6:c.455G>A ENSP00000263388.1:p.Gly152Asp
ENST00000601011.1:c.452G>A ENSP00000473138.1:p.Gly151Asp
NM_000435.2:c.455G>A NP_000426.2:p.Gly152Asp
XM_005259924.3:c.455G>A XP_005259981.1:p.Gly152Asp
XM_005259924.4:c.455G>A XP_005259981.1:p.Gly152Asp
NM_000435.3:c.455G>A MANE Select NP_000426.2:p.Gly152Asp