Canonical Allele Identifier: CA449829101
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188351G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220574G>T , CM000668.2:g.32220574G>T GRCh38
NC_000006.11:g.32188351G>T , CM000668.1:g.32188351G>T GRCh37
NC_000006.10:g.32296329G>T NCBI36
NG_028190.1:g.8494C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.990C>A MANE Select ENSP00000364163.3:p.Gly330=
ENST00000473562.1:n.1119C>A
NM_004557.3:c.990C>A NP_004548.3:p.Gly330=
NR_134949.1:n.1129C>A
NR_134950.1:n.1129C>A
NM_004557.4:c.990C>A MANE Select NP_004548.3:p.Gly330=
NR_134949.2:n.1129C>A
NR_134950.2:n.1129C>A
Search 100 bp 5'
Search 100 bp 3'