Canonical Allele Identifier: CA363557589
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188598T>A (hg19) chr6:g.32220821T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220821T>A , CM000668.2:g.32220821T>A GRCh38
NC_000006.11:g.32188598T>A , CM000668.1:g.32188598T>A GRCh37
NC_000006.10:g.32296576T>A NCBI36
NG_028190.1:g.8247A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.857A>T MANE Select ENSP00000364163.3:p.Gln286Leu
ENST00000473562.1:n.986A>T
NM_004557.3:c.857A>T NP_004548.3:p.Gln286Leu
NR_134949.1:n.996A>T
NR_134950.1:n.996A>T
NM_004557.4:c.857A>T MANE Select NP_004548.3:p.Gln286Leu
NR_134949.2:n.996A>T
NR_134950.2:n.996A>T
Search 100 bp 5'
Search 100 bp 3'