Canonical Allele Identifier: CA363557402
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188406G>T (hg19) chr6:g.32220629G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220629G>T , CM000668.2:g.32220629G>T GRCh38
NC_000006.11:g.32188406G>T , CM000668.1:g.32188406G>T GRCh37
NC_000006.10:g.32296384G>T NCBI36
NG_028190.1:g.8439C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.935C>A MANE Select ENSP00000364163.3:p.Ser312Tyr
ENST00000473562.1:n.1064C>A
NM_004557.3:c.935C>A NP_004548.3:p.Ser312Tyr
NR_134949.1:n.1074C>A
NR_134950.1:n.1074C>A
NM_004557.4:c.935C>A MANE Select NP_004548.3:p.Ser312Tyr
NR_134949.2:n.1074C>A
NR_134950.2:n.1074C>A
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