Canonical Allele Identifier: CA209320085
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs531121138
gnomAD v3: 10-70432212-G-A
gnomAD v4: 10-70432212-G-A
MyVariant Identifiers: chr10:g.72191968G>A (hg19) chr10:g.70432212G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432212G>A , CM000672.2:g.70432212G>A GRCh38
NC_000010.10:g.72191968G>A , CM000672.1:g.72191968G>A GRCh37
NC_000010.9:g.71861974G>A NCBI36
NG_012448.1:g.14498C>T
NG_012448.2:g.20737C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*724C>T MANE Select ENSP00000287139.3:n.*724C>T
NM_018055.4:c.*724C>T NP_060525.3:n.*724C>T
NM_001329906.1:c.*724C>T NP_001316835.1:n.*724C>T
NM_018055.5:c.*724C>T MANE Select NP_060525.3:n.*724C>T
NM_001329906.2:c.*724C>T NP_001316835.1:n.*724C>T
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