Canonical Allele Identifier: CA2324749982

Gene: NOTCH3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15192067C= , CM000681.2:g.15192067C=	GRCh38
NC_000019.9:g.15302878C= , CM000681.1:g.15302878C=	GRCh37
NC_000019.8:g.15163878C=	NCBI36
NG_009819.1:g.13915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.572G= MANE Select	ENSP00000263388.1:p.Gly191=
ENST00000263388.6:c.572G=	ENSP00000263388.1:p.Gly191=
ENST00000601011.1:c.569G=	ENSP00000473138.1:p.Gly190=
NM_000435.2:c.572G=	NP_000426.2:p.Gly191=
XM_005259924.3:c.572G=	XP_005259981.1:p.Gly191=
XM_005259924.4:c.572G=	XP_005259981.1:p.Gly191=
NM_000435.3:c.572G= MANE Select	NP_000426.2:p.Gly191=