Canonical Allele Identifier: CA783619532
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1490669911
gnomAD v3: 19-15187494-AC-A
gnomAD v4: 19-15187494-AC-A
MyVariant Identifiers: chr19:g.15298306del (hg19) chr19:g.15187495del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187495del , CM000681.2:g.15187495del GRCh38
NC_000019.9:g.15298306del , CM000681.1:g.15298306del GRCh37
NC_000019.8:g.15159306del NCBI36
NG_009819.1:g.18487del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-157del MANE Select ENSP00000263388.1:n.1607-157del
ENST00000263388.6:c.1607-157del ENSP00000263388.1:n.1607-157del
ENST00000601011.1:c.1604-157del ENSP00000473138.1:n.1604-157del
NM_000435.2:c.1607-157del NP_000426.2:n.1607-157del
XM_005259924.3:c.1607-157del XP_005259981.1:n.1607-157del
XM_005259924.4:c.1607-157del XP_005259981.1:n.1607-157del
NM_000435.3:c.1607-157del MANE Select NP_000426.2:n.1607-157del
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