Canonical Allele Identifier: CA2609510332
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432210-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432210C>T , CM000672.2:g.70432210C>T GRCh38
NC_000010.10:g.72191966C>T , CM000672.1:g.72191966C>T GRCh37
NC_000010.9:g.71861972C>T NCBI36
NG_012448.1:g.14500G>A
NG_012448.2:g.20739G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*726G>A MANE Select ENSP00000287139.3:n.*726G>A
NM_018055.4:c.*726G>A NP_060525.3:n.*726G>A
NM_001329906.1:c.*726G>A NP_001316835.1:n.*726G>A
NM_018055.5:c.*726G>A MANE Select NP_060525.3:n.*726G>A
NM_001329906.2:c.*726G>A NP_001316835.1:n.*726G>A
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