Canonical Allele Identifier: CA9263501
Gene: NOTCH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1934828
ClinVar RCV Id: RCV002622760
dbSNP Id: rs768216292
ExAC: 19:15297710 C / T
gnomAD v2: 19-15297710-C-T
gnomAD v4: 19-15186899-C-T
MyVariant Identifiers: chr19:g.15297710C>T (hg19) chr19:g.15186899C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186899C>T , CM000681.2:g.15186899C>T GRCh38
NC_000019.9:g.15297710C>T , CM000681.1:g.15297710C>T GRCh37
NC_000019.8:g.15158710C>T NCBI36
NG_009819.1:g.19083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1930G>A MANE Select ENSP00000263388.1:p.Val644Ile
ENST00000263388.6:c.1930G>A ENSP00000263388.1:p.Val644Ile
ENST00000601011.1:c.1927G>A ENSP00000473138.1:p.Val643Ile
NM_000435.2:c.1930G>A NP_000426.2:p.Val644Ile
XM_005259924.3:c.1930G>A XP_005259981.1:p.Val644Ile
XM_005259924.4:c.1930G>A XP_005259981.1:p.Val644Ile
NM_000435.3:c.1930G>A MANE Select NP_000426.2:p.Val644Ile
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