Canonical Allele Identifier: CA2609510333
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432211-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432211T>C , CM000672.2:g.70432211T>C GRCh38
NC_000010.10:g.72191967T>C , CM000672.1:g.72191967T>C GRCh37
NC_000010.9:g.71861973T>C NCBI36
NG_012448.1:g.14499A>G
NG_012448.2:g.20738A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*725A>G MANE Select ENSP00000287139.3:n.*725A>G
NM_018055.4:c.*725A>G NP_060525.3:n.*725A>G
NM_001329906.1:c.*725A>G NP_001316835.1:n.*725A>G
NM_018055.5:c.*725A>G MANE Select NP_060525.3:n.*725A>G
NM_001329906.2:c.*725A>G NP_001316835.1:n.*725A>G
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