Canonical Allele Identifier: CA2735638009
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1214043020

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191668C>A , CM000681.2:g.15191668C>A GRCh38
NC_000019.9:g.15302479C>A , CM000681.1:g.15302479C>A GRCh37
NC_000019.8:g.15163479C>A NCBI36
NG_009819.1:g.14314G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.803-11G>T MANE Select ENSP00000263388.1:n.803-11G>T
ENST00000263388.6:c.803-11G>T ENSP00000263388.1:n.803-11G>T
ENST00000601011.1:c.800-11G>T ENSP00000473138.1:n.800-11G>T
NM_000435.2:c.803-11G>T NP_000426.2:n.803-11G>T
XM_005259924.3:c.803-11G>T XP_005259981.1:n.803-11G>T
XM_005259924.4:c.803-11G>T XP_005259981.1:n.803-11G>T
NM_000435.3:c.803-11G>T MANE Select NP_000426.2:n.803-11G>T