Canonical Allele Identifier: CA1619468670
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32205222A= , CM000668.2:g.32205222A= GRCh38
NC_000006.11:g.32172999A= , CM000668.1:g.32172999A= GRCh37
NC_000006.10:g.32280977A= NCBI36
NG_028190.1:g.23846T=

Transcript Alleles

HGVS Amino-acid change
ENST00000375023.3:c.2866-833T= MANE Select ENSP00000364163.3:n.2866-833T=
NM_004557.3:c.2866-833T= NP_004548.3:n.2866-833T=
NR_134949.1:n.3107-833T=
NR_134950.1:n.3005-833T=
NM_004557.4:c.2866-833T= MANE Select NP_004548.3:n.2866-833T=
NR_134949.2:n.3107-833T=
NR_134950.2:n.3005-833T=