Canonical Allele Identifier: CA506078958

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15303045T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15192234T>C , CM000681.2:g.15192234T>C	GRCh38
NC_000019.9:g.15303045T>C , CM000681.1:g.15303045T>C	GRCh37
NC_000019.8:g.15164045T>C	NCBI36
NG_009819.1:g.13748A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.405A>G MANE Select	ENSP00000263388.1:p.Ser135=
ENST00000263388.6:c.405A>G	ENSP00000263388.1:p.Ser135=
ENST00000601011.1:c.402A>G	ENSP00000473138.1:p.Ser134=
NM_000435.2:c.405A>G	NP_000426.2:p.Ser135=
XM_005259924.3:c.405A>G	XP_005259981.1:p.Ser135=
XM_005259924.4:c.405A>G	XP_005259981.1:p.Ser135=
NM_000435.3:c.405A>G MANE Select	NP_000426.2:p.Ser135=