Canonical Allele Identifier: CA2609510323
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432203-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432203G>T , CM000672.2:g.70432203G>T GRCh38
NC_000010.10:g.72191959G>T , CM000672.1:g.72191959G>T GRCh37
NC_000010.9:g.71861965G>T NCBI36
NG_012448.1:g.14507C>A
NG_012448.2:g.20746C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*733C>A MANE Select ENSP00000287139.3:n.*733C>A
NM_018055.4:c.*733C>A NP_060525.3:n.*733C>A
NM_001329906.1:c.*733C>A NP_001316835.1:n.*733C>A
NM_018055.5:c.*733C>A MANE Select NP_060525.3:n.*733C>A
NM_001329906.2:c.*733C>A NP_001316835.1:n.*733C>A
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