Canonical Allele Identifier: CA2735637608
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1206641690
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191734G>C , CM000681.2:g.15191734G>C GRCh38
NC_000019.9:g.15302545G>C , CM000681.1:g.15302545G>C GRCh37
NC_000019.8:g.15163545G>C NCBI36
NG_009819.1:g.14248C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.802+11C>G MANE Select ENSP00000263388.1:n.802+11C>G
ENST00000263388.6:c.802+11C>G ENSP00000263388.1:n.802+11C>G
ENST00000601011.1:c.799+11C>G ENSP00000473138.1:n.799+11C>G
NM_000435.2:c.802+11C>G NP_000426.2:n.802+11C>G
XM_005259924.3:c.802+11C>G XP_005259981.1:n.802+11C>G
XM_005259924.4:c.802+11C>G XP_005259981.1:n.802+11C>G
NM_000435.3:c.802+11C>G MANE Select NP_000426.2:n.802+11C>G
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