Canonical Allele Identifier: CA1619472408
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1109771
gnomAD v4: 6-32219828-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32219828A>T , CM000668.2:g.32219828A>T GRCh38
NC_000006.11:g.32187605A>T , CM000668.1:g.32187605A>T GRCh37
NC_000006.10:g.32295583A>T NCBI36
NG_028190.1:g.9240T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375023.3:c.1316-42T>A MANE Select ENSP00000364163.3:n.1316-42T>A
ENST00000473562.1:n.1445-42T>A
NM_004557.3:c.1316-42T>A NP_004548.3:n.1316-42T>A
NR_134949.1:n.1455-42T>A
NR_134950.1:n.1455-42T>A
NM_004557.4:c.1316-42T>A MANE Select NP_004548.3:n.1316-42T>A
NR_134949.2:n.1455-42T>A
NR_134950.2:n.1455-42T>A
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