Canonical Allele Identifier: CA404533872
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046933431

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192156C>G , CM000681.2:g.15192156C>G GRCh38
NC_000019.9:g.15302967C>G , CM000681.1:g.15302967C>G GRCh37
NC_000019.8:g.15163967C>G NCBI36
NG_009819.1:g.13826G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.483G>C MANE Select ENSP00000263388.1:p.Glu161Asp
ENST00000263388.6:c.483G>C ENSP00000263388.1:p.Glu161Asp
ENST00000601011.1:c.480G>C ENSP00000473138.1:p.Glu160Asp
NM_000435.2:c.483G>C NP_000426.2:p.Glu161Asp
XM_005259924.3:c.483G>C XP_005259981.1:p.Glu161Asp
XM_005259924.4:c.483G>C XP_005259981.1:p.Glu161Asp
NM_000435.3:c.483G>C MANE Select NP_000426.2:p.Glu161Asp