Canonical Allele Identifier: CA632128177
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1198875827
gnomAD v2: 19-15295028-C-T
gnomAD v3: 19-15184217-C-T
gnomAD v4: 19-15184217-C-T
MyVariant Identifiers: chr19:g.15295028C>T (hg19) chr19:g.15184217C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184217C>T , CM000681.2:g.15184217C>T GRCh38
NC_000019.9:g.15295028C>T , CM000681.1:g.15295028C>T GRCh37
NC_000019.8:g.15156028C>T NCBI36
NG_009819.1:g.21765G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.2566+78G>A MANE Select ENSP00000263388.1:n.2566+78G>A
ENST00000263388.6:c.2566+78G>A ENSP00000263388.1:n.2566+78G>A
ENST00000601011.1:c.2407+689G>A ENSP00000473138.1:n.2407+689G>A
NM_000435.2:c.2566+78G>A NP_000426.2:n.2566+78G>A
XM_005259924.3:c.2410+689G>A XP_005259981.1:n.2410+689G>A
XM_005259924.4:c.2410+689G>A XP_005259981.1:n.2410+689G>A
NM_000435.3:c.2566+78G>A MANE Select NP_000426.2:n.2566+78G>A
Search 100 bp 5'
Search 100 bp 3'