Canonical Allele Identifier: CA363557571
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188590C>G (hg19) chr6:g.32220813C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220813C>G , CM000668.2:g.32220813C>G GRCh38
NC_000006.11:g.32188590C>G , CM000668.1:g.32188590C>G GRCh37
NC_000006.10:g.32296568C>G NCBI36
NG_028190.1:g.8255G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.865G>C MANE Select ENSP00000364163.3:p.Gly289Arg
ENST00000473562.1:n.994G>C
NM_004557.3:c.865G>C NP_004548.3:p.Gly289Arg
NR_134949.1:n.1004G>C
NR_134950.1:n.1004G>C
NM_004557.4:c.865G>C MANE Select NP_004548.3:p.Gly289Arg
NR_134949.2:n.1004G>C
NR_134950.2:n.1004G>C
Search 100 bp 5'
Search 100 bp 3'