Canonical Allele Identifier: CA9263160
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs752588207

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180225A>C , CM000681.2:g.15180225A>C GRCh38
NC_000019.9:g.15291036A>C , CM000681.1:g.15291036A>C GRCh37
NC_000019.8:g.15152036A>C NCBI36
NG_009819.1:g.25757T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3174T>G MANE Select ENSP00000263388.1:p.Gly1058=
ENST00000263388.6:c.3174T>G ENSP00000263388.1:p.Gly1058=
ENST00000601011.1:c.3015T>G ENSP00000473138.1:p.Gly1005=
NM_000435.2:c.3174T>G NP_000426.2:p.Gly1058=
XM_005259924.3:c.3018T>G XP_005259981.1:p.Gly1006=
XM_005259924.4:c.3018T>G XP_005259981.1:p.Gly1006=
NM_000435.3:c.3174T>G MANE Select NP_000426.2:p.Gly1058=