Canonical Allele Identifier: CA404533099
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1256940709

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191977T>C , CM000681.2:g.15191977T>C GRCh38
NC_000019.9:g.15302788T>C , CM000681.1:g.15302788T>C GRCh37
NC_000019.8:g.15163788T>C NCBI36
NG_009819.1:g.14005A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.662A>G MANE Select ENSP00000263388.1:p.Asp221Gly
ENST00000263388.6:c.662A>G ENSP00000263388.1:p.Asp221Gly
ENST00000601011.1:c.659A>G ENSP00000473138.1:p.Asp220Gly
NM_000435.2:c.662A>G NP_000426.2:p.Asp221Gly
XM_005259924.3:c.662A>G XP_005259981.1:p.Asp221Gly
XM_005259924.4:c.662A>G XP_005259981.1:p.Asp221Gly
NM_000435.3:c.662A>G MANE Select NP_000426.2:p.Asp221Gly