Canonical Allele Identifier: CA363557552
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs2127488284

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220804G>A , CM000668.2:g.32220804G>A GRCh38
NC_000006.11:g.32188581G>A , CM000668.1:g.32188581G>A GRCh37
NC_000006.10:g.32296559G>A NCBI36
NG_028190.1:g.8264C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.874C>T MANE Select ENSP00000364163.3:p.Gln292Ter
ENST00000473562.1:n.1003C>T
NM_004557.3:c.874C>T NP_004548.3:p.Gln292Ter
NR_134949.1:n.1013C>T
NR_134950.1:n.1013C>T
NM_004557.4:c.874C>T MANE Select NP_004548.3:p.Gln292Ter
NR_134949.2:n.1013C>T
NR_134950.2:n.1013C>T