Canonical Allele Identifier: CA2324750028
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192173G= , CM000681.2:g.15192173G= GRCh38
NC_000019.9:g.15302984G= , CM000681.1:g.15302984G= GRCh37
NC_000019.8:g.15163984G= NCBI36
NG_009819.1:g.13809C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.466C= MANE Select ENSP00000263388.1:p.Arg156=
ENST00000263388.6:c.466C= ENSP00000263388.1:p.Arg156=
ENST00000601011.1:c.463C= ENSP00000473138.1:p.Arg155=
NM_000435.2:c.466C= NP_000426.2:p.Arg156=
XM_005259924.3:c.466C= XP_005259981.1:p.Arg156=
XM_005259924.4:c.466C= XP_005259981.1:p.Arg156=
NM_000435.3:c.466C= MANE Select NP_000426.2:p.Arg156=