Canonical Allele Identifier: CA449829254
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs2127488234
MyVariant Identifiers: chr6:g.32188549G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220772G>A , CM000668.2:g.32220772G>A GRCh38
NC_000006.11:g.32188549G>A , CM000668.1:g.32188549G>A GRCh37
NC_000006.10:g.32296527G>A NCBI36
NG_028190.1:g.8296C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375023.3:c.906C>T MANE Select ENSP00000364163.3:p.Cys302=
ENST00000473562.1:n.1035C>T
NM_004557.3:c.906C>T NP_004548.3:p.Cys302=
NR_134949.1:n.1045C>T
NR_134950.1:n.1045C>T
NM_004557.4:c.906C>T MANE Select NP_004548.3:p.Cys302=
NR_134949.2:n.1045C>T
NR_134950.2:n.1045C>T
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