Canonical Allele Identifier: CA2324746216
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184208A= , CM000681.2:g.15184208A= GRCh38
NC_000019.9:g.15295019A= , CM000681.1:g.15295019A= GRCh37
NC_000019.8:g.15156019A= NCBI36
NG_009819.1:g.21774T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.2566+87T= MANE Select ENSP00000263388.1:n.2566+87T=
ENST00000263388.6:c.2566+87T= ENSP00000263388.1:n.2566+87T=
ENST00000601011.1:c.2407+698T= ENSP00000473138.1:n.2407+698T=
NM_000435.2:c.2566+87T= NP_000426.2:n.2566+87T=
XM_005259924.3:c.2410+698T= XP_005259981.1:n.2410+698T=
XM_005259924.4:c.2410+698T= XP_005259981.1:n.2410+698T=
NM_000435.3:c.2566+87T= MANE Select NP_000426.2:n.2566+87T=
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