Canonical Allele Identifier: CA363557181
Gene: NOTCH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32188308T>A (hg19) chr6:g.32220531T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220531T>A , CM000668.2:g.32220531T>A GRCh38
NC_000006.11:g.32188308T>A , CM000668.1:g.32188308T>A GRCh37
NC_000006.10:g.32296286T>A NCBI36
NG_028190.1:g.8537A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.1033A>T MANE Select ENSP00000364163.3:p.Ser345Cys
ENST00000473562.1:n.1162A>T
NM_004557.3:c.1033A>T NP_004548.3:p.Ser345Cys
NR_134949.1:n.1172A>T
NR_134950.1:n.1172A>T
NM_004557.4:c.1033A>T MANE Select NP_004548.3:p.Ser345Cys
NR_134949.2:n.1172A>T
NR_134950.2:n.1172A>T
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