Canonical Allele Identifier: CA2324749928
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191968C= , CM000681.2:g.15191968C= GRCh38
NC_000019.9:g.15302779C= , CM000681.1:g.15302779C= GRCh37
NC_000019.8:g.15163779C= NCBI36
NG_009819.1:g.14014G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.671G= MANE Select ENSP00000263388.1:p.Cys224=
ENST00000263388.6:c.671G= ENSP00000263388.1:p.Cys224=
ENST00000601011.1:c.668G= ENSP00000473138.1:p.Cys223=
NM_000435.2:c.671G= NP_000426.2:p.Cys224=
XM_005259924.3:c.671G= XP_005259981.1:p.Cys224=
XM_005259924.4:c.671G= XP_005259981.1:p.Cys224=
NM_000435.3:c.671G= MANE Select NP_000426.2:p.Cys224=