Canonical Allele Identifier: CA2609510314
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432194-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432194C>G , CM000672.2:g.70432194C>G GRCh38
NC_000010.10:g.72191950C>G , CM000672.1:g.72191950C>G GRCh37
NC_000010.9:g.71861956C>G NCBI36
NG_012448.1:g.14516G>C
NG_012448.2:g.20755G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*742G>C MANE Select ENSP00000287139.3:n.*742G>C
NM_018055.4:c.*742G>C NP_060525.3:n.*742G>C
NM_001329906.1:c.*742G>C NP_001316835.1:n.*742G>C
NM_018055.5:c.*742G>C MANE Select NP_060525.3:n.*742G>C
NM_001329906.2:c.*742G>C NP_001316835.1:n.*742G>C
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