Canonical Allele Identifier: CA506078388

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15297744T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15186933T>C , CM000681.2:g.15186933T>C	GRCh38
NC_000019.9:g.15297744T>C , CM000681.1:g.15297744T>C	GRCh37
NC_000019.8:g.15158744T>C	NCBI36
NG_009819.1:g.19049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.1896A>G MANE Select	ENSP00000263388.1:p.Gly632=
ENST00000263388.6:c.1896A>G	ENSP00000263388.1:p.Gly632=
ENST00000601011.1:c.1893A>G	ENSP00000473138.1:p.Gly631=
NM_000435.2:c.1896A>G	NP_000426.2:p.Gly632=
XM_005259924.3:c.1896A>G	XP_005259981.1:p.Gly632=
XM_005259924.4:c.1896A>G	XP_005259981.1:p.Gly632=
NM_000435.3:c.1896A>G MANE Select	NP_000426.2:p.Gly632=