Canonical Allele Identifier: CA470038827
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70441557-C-T
MyVariant Identifiers: chr10:g.72201313C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70441557C>T , CM000672.2:g.70441557C>T GRCh38
NC_000010.10:g.72201313C>T , CM000672.1:g.72201313C>T GRCh37
NC_000010.9:g.71871319C>T NCBI36
NG_012448.1:g.5153G>A
NG_012448.2:g.11392G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.111G>A MANE Select ENSP00000287139.3:p.Ser37=
ENST00000287139.7:c.111G>A ENSP00000287139.3:p.Ser37=
ENST00000414871.1:c.29-5574G>A ENSP00000394468.1:n.29-5574G>A
NM_018055.4:c.111G>A NP_060525.3:p.Ser37=
NM_001329906.1:c.-206-5574G>A NP_001316835.1:n.-206-5574G>A
XM_024448028.1:c.-207+474G>A XP_024303796.1:n.-207+474G>A
NM_018055.5:c.111G>A MANE Select NP_060525.3:p.Ser37=
NM_001329906.2:c.-206-5574G>A NP_001316835.1:n.-206-5574G>A
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