Canonical Allele Identifier: CA2324749851
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191799T= , CM000681.2:g.15191799T= GRCh38
NC_000019.9:g.15302610T= , CM000681.1:g.15302610T= GRCh37
NC_000019.8:g.15163610T= NCBI36
NG_009819.1:g.14183A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.748A= MANE Select ENSP00000263388.1:p.Thr250=
ENST00000263388.6:c.748A= ENSP00000263388.1:p.Thr250=
ENST00000601011.1:c.745A= ENSP00000473138.1:p.Thr249=
NM_000435.2:c.748A= NP_000426.2:p.Thr250=
XM_005259924.3:c.748A= XP_005259981.1:p.Thr250=
XM_005259924.4:c.748A= XP_005259981.1:p.Thr250=
NM_000435.3:c.748A= MANE Select NP_000426.2:p.Thr250=