Canonical Allele Identifier: CA404534142
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1174625611

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192218G>T , CM000681.2:g.15192218G>T GRCh38
NC_000019.9:g.15303029G>T , CM000681.1:g.15303029G>T GRCh37
NC_000019.8:g.15164029G>T NCBI36
NG_009819.1:g.13764C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.421C>A MANE Select ENSP00000263388.1:p.Arg141Ser
ENST00000263388.6:c.421C>A ENSP00000263388.1:p.Arg141Ser
ENST00000601011.1:c.418C>A ENSP00000473138.1:p.Arg140Ser
NM_000435.2:c.421C>A NP_000426.2:p.Arg141Ser
XM_005259924.3:c.421C>A XP_005259981.1:p.Arg141Ser
XM_005259924.4:c.421C>A XP_005259981.1:p.Arg141Ser
NM_000435.3:c.421C>A MANE Select NP_000426.2:p.Arg141Ser