Canonical Allele Identifier: CA9263838
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs756520455
ExAC: 19:15302801 C / T
gnomAD v2: 19-15302801-C-T
gnomAD v3: 19-15191990-C-T
gnomAD v4: 19-15191990-C-T
COSMIC: COSM1217625 COSM1217626
MyVariant Identifiers: chr19:g.15302801C>T (hg19) chr19:g.15191990C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191990C>T , CM000681.2:g.15191990C>T GRCh38
NC_000019.9:g.15302801C>T , CM000681.1:g.15302801C>T GRCh37
NC_000019.8:g.15163801C>T NCBI36
NG_009819.1:g.13992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.649G>A MANE Select ENSP00000263388.1:p.Asp217Asn
ENST00000263388.6:c.649G>A ENSP00000263388.1:p.Asp217Asn
ENST00000601011.1:c.646G>A ENSP00000473138.1:p.Asp216Asn
NM_000435.2:c.649G>A NP_000426.2:p.Asp217Asn
XM_005259924.3:c.649G>A XP_005259981.1:p.Asp217Asn
XM_005259924.4:c.649G>A XP_005259981.1:p.Asp217Asn
NM_000435.3:c.649G>A MANE Select NP_000426.2:p.Asp217Asn
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