Canonical Allele Identifier: CA632128052
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1472638791

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187040G>T , CM000681.2:g.15187040G>T GRCh38
NC_000019.9:g.15297851G>T , CM000681.1:g.15297851G>T GRCh37
NC_000019.8:g.15158851G>T NCBI36
NG_009819.1:g.18942C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1841-52C>A MANE Select ENSP00000263388.1:n.1841-52C>A
ENST00000263388.6:c.1841-52C>A ENSP00000263388.1:n.1841-52C>A
ENST00000601011.1:c.1838-52C>A ENSP00000473138.1:n.1838-52C>A
NM_000435.2:c.1841-52C>A NP_000426.2:n.1841-52C>A
XM_005259924.3:c.1841-52C>A XP_005259981.1:n.1841-52C>A
XM_005259924.4:c.1841-52C>A XP_005259981.1:n.1841-52C>A
NM_000435.3:c.1841-52C>A MANE Select NP_000426.2:n.1841-52C>A