Canonical Allele Identifier: CA449728674
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1272872434
gnomAD v4: 6-32222611-C-T
MyVariant Identifiers: chr6:g.32190388C>T (hg19) chr6:g.32222611C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32222611C>T , CM000668.2:g.32222611C>T GRCh38
NC_000006.11:g.32190388C>T , CM000668.1:g.32190388C>T GRCh37
NC_000006.10:g.32298366C>T NCBI36
NG_028190.1:g.6457G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.351G>A MANE Select ENSP00000364163.3:p.Lys117=
ENST00000473562.1:n.480G>A
NM_004557.3:c.351G>A NP_004548.3:p.Lys117=
NR_134949.1:n.490G>A
NR_134950.1:n.490G>A
NM_004557.4:c.351G>A MANE Select NP_004548.3:p.Lys117=
NR_134949.2:n.490G>A
NR_134950.2:n.490G>A
Search 100 bp 5'
Search 100 bp 3'