Canonical Allele Identifier: CA404533869
Gene: NOTCH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1701358
ClinVar RCV Id: RCV002276065
dbSNP Id: rs2145441998
gnomAD v4: 19-15192155-A-G
MyVariant Identifiers: chr19:g.15302966A>G (hg19) chr19:g.15192155A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192155A>G , CM000681.2:g.15192155A>G GRCh38
NC_000019.9:g.15302966A>G , CM000681.1:g.15302966A>G GRCh37
NC_000019.8:g.15163966A>G NCBI36
NG_009819.1:g.13827T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.484T>C MANE Select ENSP00000263388.1:p.Cys162Arg
ENST00000263388.6:c.484T>C ENSP00000263388.1:p.Cys162Arg
ENST00000601011.1:c.481T>C ENSP00000473138.1:p.Cys161Arg
NM_000435.2:c.484T>C NP_000426.2:p.Cys162Arg
XM_005259924.3:c.484T>C XP_005259981.1:p.Cys162Arg
XM_005259924.4:c.484T>C XP_005259981.1:p.Cys162Arg
NM_000435.3:c.484T>C MANE Select NP_000426.2:p.Cys162Arg
Search 100 bp 5'
Search 100 bp 3'