Canonical Allele Identifier: CA363557410
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1789700044

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220632C>T , CM000668.2:g.32220632C>T GRCh38
NC_000006.11:g.32188409C>T , CM000668.1:g.32188409C>T GRCh37
NC_000006.10:g.32296387C>T NCBI36
NG_028190.1:g.8436G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.932G>A MANE Select ENSP00000364163.3:p.Cys311Tyr
ENST00000473562.1:n.1061G>A
NM_004557.3:c.932G>A NP_004548.3:p.Cys311Tyr
NR_134949.1:n.1071G>A
NR_134950.1:n.1071G>A
NM_004557.4:c.932G>A MANE Select NP_004548.3:p.Cys311Tyr
NR_134949.2:n.1071G>A
NR_134950.2:n.1071G>A