Canonical Allele Identifier: CA404519316
Gene: NOTCH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15295151A>T (hg19) chr19:g.15184340A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184340A>T , CM000681.2:g.15184340A>T GRCh38
NC_000019.9:g.15295151A>T , CM000681.1:g.15295151A>T GRCh37
NC_000019.8:g.15156151A>T NCBI36
NG_009819.1:g.21642T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.2521T>A MANE Select ENSP00000263388.1:p.Tyr841Asn
ENST00000263388.6:c.2521T>A ENSP00000263388.1:p.Tyr841Asn
ENST00000601011.1:c.2407+566T>A ENSP00000473138.1:n.2407+566T>A
NM_000435.2:c.2521T>A NP_000426.2:p.Tyr841Asn
XM_005259924.3:c.2410+566T>A XP_005259981.1:n.2410+566T>A
XM_005259924.4:c.2410+566T>A XP_005259981.1:n.2410+566T>A
NM_000435.3:c.2521T>A MANE Select NP_000426.2:p.Tyr841Asn
Search 100 bp 5'
Search 100 bp 3'