Canonical Allele Identifier: CA404513130

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15290929T>C (hg19) ; chr19:g.15180118T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180118T>C , CM000681.2:g.15180118T>C	GRCh38
NC_000019.9:g.15290929T>C , CM000681.1:g.15290929T>C	GRCh37
NC_000019.8:g.15151929T>C	NCBI36
NG_009819.1:g.25864A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263388.7:c.3281A>G MANE Select	ENSP00000263388.1:p.Gln1094Arg
ENST00000263388.6:c.3281A>G	ENSP00000263388.1:p.Gln1094Arg
ENST00000601011.1:c.3122A>G	ENSP00000473138.1:p.Gln1041Arg
NM_000435.2:c.3281A>G	NP_000426.2:p.Gln1094Arg
XM_005259924.3:c.3125A>G	XP_005259981.1:p.Gln1042Arg
XM_005259924.4:c.3125A>G	XP_005259981.1:p.Gln1042Arg
NM_000435.3:c.3281A>G MANE Select	NP_000426.2:p.Gln1094Arg