Canonical Allele Identifier: CA2324744246
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180114A= , CM000681.2:g.15180114A= GRCh38
NC_000019.9:g.15290925A= , CM000681.1:g.15290925A= GRCh37
NC_000019.8:g.15151925A= NCBI36
NG_009819.1:g.25868T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3285T= MANE Select ENSP00000263388.1:p.His1095=
ENST00000263388.6:c.3285T= ENSP00000263388.1:p.His1095=
ENST00000601011.1:c.3126T= ENSP00000473138.1:p.His1042=
NM_000435.2:c.3285T= NP_000426.2:p.His1095=
XM_005259924.3:c.3129T= XP_005259981.1:p.His1043=
XM_005259924.4:c.3129T= XP_005259981.1:p.His1043=
NM_000435.3:c.3285T= MANE Select NP_000426.2:p.His1095=