Canonical Allele Identifier: CA506077931
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs200504060
MyVariant Identifiers: chr19:g.15290031G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15179220G>T , CM000681.2:g.15179220G>T GRCh38
NC_000019.9:g.15290031G>T , CM000681.1:g.15290031G>T GRCh37
NC_000019.8:g.15151031G>T NCBI36
NG_009819.1:g.26762C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3523C>A MANE Select ENSP00000263388.1:p.Arg1175=
ENST00000263388.6:c.3523C>A ENSP00000263388.1:p.Arg1175=
ENST00000595045.1:n.359C>A
ENST00000600841.1:n.1C>A
ENST00000601011.1:c.3364C>A ENSP00000473138.1:p.Arg1122=
NM_000435.2:c.3523C>A NP_000426.2:p.Arg1175=
XM_005259924.3:c.3367C>A XP_005259981.1:p.Arg1123=
XM_005259924.4:c.3367C>A XP_005259981.1:p.Arg1123=
NM_000435.3:c.3523C>A MANE Select NP_000426.2:p.Arg1175=