Canonical Allele Identifier: CA2324744174
Gene: NOTCH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15179983T= , CM000681.2:g.15179983T= GRCh38
NC_000019.9:g.15290794T= , CM000681.1:g.15290794T= GRCh37
NC_000019.8:g.15151794T= NCBI36
NG_009819.1:g.25999A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+89A= MANE Select ENSP00000263388.1:n.3327+89A=
ENST00000263388.6:c.3327+89A= ENSP00000263388.1:n.3327+89A=
ENST00000601011.1:c.3168+89A= ENSP00000473138.1:n.3168+89A=
NM_000435.2:c.3327+89A= NP_000426.2:n.3327+89A=
XM_005259924.3:c.3171+89A= XP_005259981.1:n.3171+89A=
XM_005259924.4:c.3171+89A= XP_005259981.1:n.3171+89A=
NM_000435.3:c.3327+89A= MANE Select NP_000426.2:n.3327+89A=
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