Canonical Allele Identifier: CA2324750037
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192189G= , CM000681.2:g.15192189G= GRCh38
NC_000019.9:g.15303000G= , CM000681.1:g.15303000G= GRCh37
NC_000019.8:g.15164000G= NCBI36
NG_009819.1:g.13793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.450C= MANE Select ENSP00000263388.1:p.Tyr150=
ENST00000263388.6:c.450C= ENSP00000263388.1:p.Tyr150=
ENST00000601011.1:c.447C= ENSP00000473138.1:p.Tyr149=
NM_000435.2:c.450C= NP_000426.2:p.Tyr150=
XM_005259924.3:c.450C= XP_005259981.1:p.Tyr150=
XM_005259924.4:c.450C= XP_005259981.1:p.Tyr150=
NM_000435.3:c.450C= MANE Select NP_000426.2:p.Tyr150=