Canonical Allele Identifier: CA404533839
Gene: NOTCH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15302953T>G (hg19) chr19:g.15192142T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192142T>G , CM000681.2:g.15192142T>G GRCh38
NC_000019.9:g.15302953T>G , CM000681.1:g.15302953T>G GRCh37
NC_000019.8:g.15163953T>G NCBI36
NG_009819.1:g.13840A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.497A>C MANE Select ENSP00000263388.1:p.Glu166Ala
ENST00000263388.6:c.497A>C ENSP00000263388.1:p.Glu166Ala
ENST00000601011.1:c.494A>C ENSP00000473138.1:p.Glu165Ala
NM_000435.2:c.497A>C NP_000426.2:p.Glu166Ala
XM_005259924.3:c.497A>C XP_005259981.1:p.Glu166Ala
XM_005259924.4:c.497A>C XP_005259981.1:p.Glu166Ala
NM_000435.3:c.497A>C MANE Select NP_000426.2:p.Glu166Ala
Search 100 bp 5'
Search 100 bp 3'