Canonical Allele Identifier: CA2735796059
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145421281
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180641T>G , CM000681.2:g.15180641T>G GRCh38
NC_000019.9:g.15291452T>G , CM000681.1:g.15291452T>G GRCh37
NC_000019.8:g.15152452T>G NCBI36
NG_009819.1:g.25341A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3142+40A>C MANE Select ENSP00000263388.1:n.3142+40A>C
ENST00000263388.6:c.3142+40A>C ENSP00000263388.1:n.3142+40A>C
ENST00000601011.1:c.2983+40A>C ENSP00000473138.1:n.2983+40A>C
NM_000435.2:c.3142+40A>C NP_000426.2:n.3142+40A>C
XM_005259924.3:c.2986+40A>C XP_005259981.1:n.2986+40A>C
XM_005259924.4:c.2986+40A>C XP_005259981.1:n.2986+40A>C
NM_000435.3:c.3142+40A>C MANE Select NP_000426.2:n.3142+40A>C
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