Canonical Allele Identifier: CA2324747539
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186949T= , CM000681.2:g.15186949T= GRCh38
NC_000019.9:g.15297760T= , CM000681.1:g.15297760T= GRCh37
NC_000019.8:g.15158760T= NCBI36
NG_009819.1:g.19033A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1880A= MANE Select ENSP00000263388.1:p.Asn627=
ENST00000263388.6:c.1880A= ENSP00000263388.1:p.Asn627=
ENST00000601011.1:c.1877A= ENSP00000473138.1:p.Asn626=
NM_000435.2:c.1880A= NP_000426.2:p.Asn627=
XM_005259924.3:c.1880A= XP_005259981.1:p.Asn627=
XM_005259924.4:c.1880A= XP_005259981.1:p.Asn627=
NM_000435.3:c.1880A= MANE Select NP_000426.2:p.Asn627=