Canonical Allele Identifier: CA10582732
Gene: NODAL HGNC NCBI

Linked Data

ClinVar Variation Id: 241245
ClinVar RCV Id: RCV000231796
dbSNP Id: rs878855044
gnomAD v3: 10-70435285-C-T
gnomAD v4: 10-70435285-C-T
MyVariant Identifiers: chr10:g.72195041C>T (hg19) chr10:g.70435285C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435285C>T , CM000672.2:g.70435285C>T GRCh38
NC_000010.10:g.72195041C>T , CM000672.1:g.72195041C>T GRCh37
NC_000010.9:g.71865047C>T NCBI36
NG_012448.1:g.11425G>A
NG_012448.2:g.17664G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.891+1G>A MANE Select ENSP00000287139.3:n.891+1G>A
ENST00000287139.7:c.891+1G>A ENSP00000287139.3:n.891+1G>A
ENST00000414871.1:c.726+1G>A ENSP00000394468.1:n.726+1G>A
NM_018055.4:c.891+1G>A NP_060525.3:n.891+1G>A
NM_001329906.1:c.492+1G>A NP_001316835.1:n.492+1G>A
XM_024448028.1:c.492+1G>A XP_024303796.1:n.492+1G>A
NM_018055.5:c.891+1G>A MANE Select NP_060525.3:n.891+1G>A
NM_001329906.2:c.492+1G>A NP_001316835.1:n.492+1G>A
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