Canonical Allele Identifier: CA404534001

Gene: NOTCH3

Linked Data

• dbSNP Id: rs371491165
• MyVariant Identifiers: chr19:g.15302999G>T (hg19) ; chr19:g.15192188G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15192188G>T , CM000681.2:g.15192188G>T	GRCh38
NC_000019.9:g.15302999G>T , CM000681.1:g.15302999G>T	GRCh37
NC_000019.8:g.15163999G>T	NCBI36
NG_009819.1:g.13794C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.451C>A MANE Select	ENSP00000263388.1:p.Gln151Lys
ENST00000263388.6:c.451C>A	ENSP00000263388.1:p.Gln151Lys
ENST00000601011.1:c.448C>A	ENSP00000473138.1:p.Gln150Lys
NM_000435.2:c.451C>A	NP_000426.2:p.Gln151Lys
XM_005259924.3:c.451C>A	XP_005259981.1:p.Gln151Lys
XM_005259924.4:c.451C>A	XP_005259981.1:p.Gln151Lys
NM_000435.3:c.451C>A MANE Select	NP_000426.2:p.Gln151Lys