Canonical Allele Identifier: CA404532920
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145440899

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191858C>T , CM000681.2:g.15191858C>T GRCh38
NC_000019.9:g.15302669C>T , CM000681.1:g.15302669C>T GRCh37
NC_000019.8:g.15163669C>T NCBI36
NG_009819.1:g.14124G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.689G>A MANE Select ENSP00000263388.1:p.Gly230Asp
ENST00000263388.6:c.689G>A ENSP00000263388.1:p.Gly230Asp
ENST00000601011.1:c.686G>A ENSP00000473138.1:p.Gly229Asp
NM_000435.2:c.689G>A NP_000426.2:p.Gly230Asp
XM_005259924.3:c.689G>A XP_005259981.1:p.Gly230Asp
XM_005259924.4:c.689G>A XP_005259981.1:p.Gly230Asp
NM_000435.3:c.689G>A MANE Select NP_000426.2:p.Gly230Asp