Canonical Allele Identifier: CA1918248404
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs2279253
gnomAD v4: 10-70432196-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432196A>T , CM000672.2:g.70432196A>T GRCh38
NC_000010.10:g.72191952A>T , CM000672.1:g.72191952A>T GRCh37
NC_000010.9:g.71861958A>T NCBI36
NG_012448.1:g.14514T>A
NG_012448.2:g.20753T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*740T>A MANE Select ENSP00000287139.3:n.*740T>A
NM_018055.4:c.*740T>A NP_060525.3:n.*740T>A
NM_001329906.1:c.*740T>A NP_001316835.1:n.*740T>A
NM_018055.5:c.*740T>A MANE Select NP_060525.3:n.*740T>A
NM_001329906.2:c.*740T>A NP_001316835.1:n.*740T>A
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