Canonical Allele Identifier: CA449829317
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188591C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220814C>A , CM000668.2:g.32220814C>A GRCh38
NC_000006.11:g.32188591C>A , CM000668.1:g.32188591C>A GRCh37
NC_000006.10:g.32296569C>A NCBI36
NG_028190.1:g.8254G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.864G>T MANE Select ENSP00000364163.3:p.Gly288=
ENST00000473562.1:n.993G>T
NM_004557.3:c.864G>T NP_004548.3:p.Gly288=
NR_134949.1:n.1003G>T
NR_134950.1:n.1003G>T
NM_004557.4:c.864G>T MANE Select NP_004548.3:p.Gly288=
NR_134949.2:n.1003G>T
NR_134950.2:n.1003G>T