Canonical Allele Identifier: CA404524034

Gene: NOTCH3

Linked Data

• gnomAD v4: 19-15186905-C-A
• MyVariant Identifiers: chr19:g.15297716C>A (hg19) ; chr19:g.15186905C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15186905C>A , CM000681.2:g.15186905C>A	GRCh38
NC_000019.9:g.15297716C>A , CM000681.1:g.15297716C>A	GRCh37
NC_000019.8:g.15158716C>A	NCBI36
NG_009819.1:g.19077G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.1924G>T MANE Select	ENSP00000263388.1:p.Asp642Tyr
ENST00000263388.6:c.1924G>T	ENSP00000263388.1:p.Asp642Tyr
ENST00000601011.1:c.1921G>T	ENSP00000473138.1:p.Asp641Tyr
NM_000435.2:c.1924G>T	NP_000426.2:p.Asp642Tyr
XM_005259924.3:c.1924G>T	XP_005259981.1:p.Asp642Tyr
XM_005259924.4:c.1924G>T	XP_005259981.1:p.Asp642Tyr
NM_000435.3:c.1924G>T MANE Select	NP_000426.2:p.Asp642Tyr