Canonical Allele Identifier: CA2324744196
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180027A= , CM000681.2:g.15180027A= GRCh38
NC_000019.9:g.15290838A= , CM000681.1:g.15290838A= GRCh37
NC_000019.8:g.15151838A= NCBI36
NG_009819.1:g.25955T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+45T= MANE Select ENSP00000263388.1:n.3327+45T=
ENST00000263388.6:c.3327+45T= ENSP00000263388.1:n.3327+45T=
ENST00000601011.1:c.3168+45T= ENSP00000473138.1:n.3168+45T=
NM_000435.2:c.3327+45T= NP_000426.2:n.3327+45T=
XM_005259924.3:c.3171+45T= XP_005259981.1:n.3171+45T=
XM_005259924.4:c.3171+45T= XP_005259981.1:n.3171+45T=
NM_000435.3:c.3327+45T= MANE Select NP_000426.2:n.3327+45T=
Search 100 bp 5'
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