Canonical Allele Identifier: CA136900223
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs981071686
gnomAD v4: 6-32202802-G-C
MyVariant Identifiers: chr6:g.32170579G>C (hg19) chr6:g.32202802G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202802G>C , CM000668.2:g.32202802G>C GRCh38
NC_000006.11:g.32170579G>C , CM000668.1:g.32170579G>C GRCh37
NC_000006.10:g.32278557G>C NCBI36
NG_028190.1:g.26266C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-203C>G MANE Select ENSP00000364163.3:n.3232-203C>G
ENST00000474612.1:n.1115C>G
NM_004557.3:c.3232-203C>G NP_004548.3:n.3232-203C>G
NR_134949.1:n.3472+968C>G
NR_134950.1:n.3370+968C>G
NM_004557.4:c.3232-203C>G MANE Select NP_004548.3:n.3232-203C>G
NR_134949.2:n.3472+968C>G
NR_134950.2:n.3370+968C>G
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