Canonical Allele Identifier: CA404533980

Gene: NOTCH3

Linked Data

• dbSNP Id: rs2046933881
• MyVariant Identifiers: chr19:g.15302996C>T (hg19) ; chr19:g.15192185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15192185C>T , CM000681.2:g.15192185C>T	GRCh38
NC_000019.9:g.15302996C>T , CM000681.1:g.15302996C>T	GRCh37
NC_000019.8:g.15163996C>T	NCBI36
NG_009819.1:g.13797G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.454G>A MANE Select	ENSP00000263388.1:p.Gly152Ser
ENST00000263388.6:c.454G>A	ENSP00000263388.1:p.Gly152Ser
ENST00000601011.1:c.451G>A	ENSP00000473138.1:p.Gly151Ser
NM_000435.2:c.454G>A	NP_000426.2:p.Gly152Ser
XM_005259924.3:c.454G>A	XP_005259981.1:p.Gly152Ser
XM_005259924.4:c.454G>A	XP_005259981.1:p.Gly152Ser
NM_000435.3:c.454G>A MANE Select	NP_000426.2:p.Gly152Ser