Canonical Allele Identifier: CA363558906
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs2127491052
MyVariant Identifiers: chr6:g.32190486G>T (hg19) chr6:g.32222709G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32222709G>T , CM000668.2:g.32222709G>T GRCh38
NC_000006.11:g.32190486G>T , CM000668.1:g.32190486G>T GRCh37
NC_000006.10:g.32298464G>T NCBI36
NG_028190.1:g.6359C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.253C>A MANE Select ENSP00000364163.3:p.Pro85Thr
ENST00000473562.1:n.382C>A
NM_004557.3:c.253C>A NP_004548.3:p.Pro85Thr
NR_134949.1:n.392C>A
NR_134950.1:n.392C>A
NM_004557.4:c.253C>A MANE Select NP_004548.3:p.Pro85Thr
NR_134949.2:n.392C>A
NR_134950.2:n.392C>A
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