Canonical Allele Identifier: CA505824223

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15290919C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180108C>T , CM000681.2:g.15180108C>T	GRCh38
NC_000019.9:g.15290919C>T , CM000681.1:g.15290919C>T	GRCh37
NC_000019.8:g.15151919C>T	NCBI36
NG_009819.1:g.25874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.3291G>A MANE Select	ENSP00000263388.1:p.Gly1097=
ENST00000263388.6:c.3291G>A	ENSP00000263388.1:p.Gly1097=
ENST00000601011.1:c.3132G>A	ENSP00000473138.1:p.Gly1044=
NM_000435.2:c.3291G>A	NP_000426.2:p.Gly1097=
XM_005259924.3:c.3135G>A	XP_005259981.1:p.Gly1045=
XM_005259924.4:c.3135G>A	XP_005259981.1:p.Gly1045=
NM_000435.3:c.3291G>A MANE Select	NP_000426.2:p.Gly1097=