Canonical Allele Identifier: CA2324744268
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180168A= , CM000681.2:g.15180168A= GRCh38
NC_000019.9:g.15290979A= , CM000681.1:g.15290979A= GRCh37
NC_000019.8:g.15151979A= NCBI36
NG_009819.1:g.25814T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3231T= MANE Select ENSP00000263388.1:p.Thr1077=
ENST00000263388.6:c.3231T= ENSP00000263388.1:p.Thr1077=
ENST00000601011.1:c.3072T= ENSP00000473138.1:p.Thr1024=
NM_000435.2:c.3231T= NP_000426.2:p.Thr1077=
XM_005259924.3:c.3075T= XP_005259981.1:p.Thr1025=
XM_005259924.4:c.3075T= XP_005259981.1:p.Thr1025=
NM_000435.3:c.3231T= MANE Select NP_000426.2:p.Thr1077=