Canonical Allele Identifier: CA667993309
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs1196418389
gnomAD v3: 10-70432206-G-C
gnomAD v4: 10-70432206-G-C
MyVariant Identifiers: chr10:g.72191962G>C (hg19) chr10:g.70432206G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432206G>C , CM000672.2:g.70432206G>C GRCh38
NC_000010.10:g.72191962G>C , CM000672.1:g.72191962G>C GRCh37
NC_000010.9:g.71861968G>C NCBI36
NG_012448.1:g.14504C>G
NG_012448.2:g.20743C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*730C>G MANE Select ENSP00000287139.3:n.*730C>G
NM_018055.4:c.*730C>G NP_060525.3:n.*730C>G
NM_001329906.1:c.*730C>G NP_001316835.1:n.*730C>G
NM_018055.5:c.*730C>G MANE Select NP_060525.3:n.*730C>G
NM_001329906.2:c.*730C>G NP_001316835.1:n.*730C>G
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