Canonical Allele Identifier: CA2813714759
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15179919C>A , CM000681.2:g.15179919C>A GRCh38
NC_000019.9:g.15290730C>A , CM000681.1:g.15290730C>A GRCh37
NC_000019.8:g.15151730C>A NCBI36
NG_009819.1:g.26063G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+153G>T MANE Select ENSP00000263388.1:n.3327+153G>T
ENST00000263388.6:c.3327+153G>T ENSP00000263388.1:n.3327+153G>T
ENST00000601011.1:c.3168+153G>T ENSP00000473138.1:n.3168+153G>T
NM_000435.2:c.3327+153G>T NP_000426.2:n.3327+153G>T
XM_005259924.3:c.3171+153G>T XP_005259981.1:n.3171+153G>T
XM_005259924.4:c.3171+153G>T XP_005259981.1:n.3171+153G>T
NM_000435.3:c.3327+153G>T MANE Select NP_000426.2:n.3327+153G>T