Canonical Allele Identifier: CA9263859
Gene: NOTCH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 772302
ClinVar RCV Id: RCV000951823
dbSNP Id: rs367943979
ExAC: 19:15302859 G / A
gnomAD v2: 19-15302859-G-A
gnomAD v3: 19-15192048-G-A
gnomAD v4: 19-15192048-G-A
MyVariant Identifiers: chr19:g.15302859G>A (hg19) chr19:g.15192048G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192048G>A , CM000681.2:g.15192048G>A GRCh38
NC_000019.9:g.15302859G>A , CM000681.1:g.15302859G>A GRCh37
NC_000019.8:g.15163859G>A NCBI36
NG_009819.1:g.13934C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.591C>T MANE Select ENSP00000263388.1:p.Pro197=
ENST00000263388.6:c.591C>T ENSP00000263388.1:p.Pro197=
ENST00000601011.1:c.588C>T ENSP00000473138.1:p.Pro196=
NM_000435.2:c.591C>T NP_000426.2:p.Pro197=
XM_005259924.3:c.591C>T XP_005259981.1:p.Pro197=
XM_005259924.4:c.591C>T XP_005259981.1:p.Pro197=
NM_000435.3:c.591C>T MANE Select NP_000426.2:p.Pro197=
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