Canonical Allele Identifier: CA3740087
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs561687277
ExAC: 6:32188296 C / T
gnomAD v2: 6-32188296-C-T
gnomAD v3: 6-32220519-C-T
gnomAD v4: 6-32220519-C-T
COSMIC: COSM3928362
MyVariant Identifiers: chr6:g.32188296C>T (hg19) chr6:g.32188296_32188297delinsTG (hg19) chr6:g.32220519C>T (hg38) chr6:g.32220519_32220520delinsTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220519C>T , CM000668.2:g.32220519C>T GRCh38
NC_000006.11:g.32188296C>T , CM000668.1:g.32188296C>T GRCh37
NC_000006.10:g.32296274C>T NCBI36
NG_028190.1:g.8549G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.1045G>A MANE Select ENSP00000364163.3:p.Gly349Ser
ENST00000473562.1:n.1174G>A
NM_004557.3:c.1045G>A NP_004548.3:p.Gly349Ser
NR_134949.1:n.1184G>A
NR_134950.1:n.1184G>A
NM_004557.4:c.1045G>A MANE Select NP_004548.3:p.Gly349Ser
NR_134949.2:n.1184G>A
NR_134950.2:n.1184G>A
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