Canonical Allele Identifier: CA2813714785
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180581A>C , CM000681.2:g.15180581A>C GRCh38
NC_000019.9:g.15291392A>C , CM000681.1:g.15291392A>C GRCh37
NC_000019.8:g.15152392A>C NCBI36
NG_009819.1:g.25401T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3142+100T>G MANE Select ENSP00000263388.1:n.3142+100T>G
ENST00000263388.6:c.3142+100T>G ENSP00000263388.1:n.3142+100T>G
ENST00000601011.1:c.2983+100T>G ENSP00000473138.1:n.2983+100T>G
NM_000435.2:c.3142+100T>G NP_000426.2:n.3142+100T>G
XM_005259924.3:c.2986+100T>G XP_005259981.1:n.2986+100T>G
XM_005259924.4:c.2986+100T>G XP_005259981.1:n.2986+100T>G
NM_000435.3:c.3142+100T>G MANE Select NP_000426.2:n.3142+100T>G