Canonical Allele Identifier: CA5537561
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs751938859
ExAC: 10:72195310 C / T
gnomAD v2: 10-72195310-C-T
gnomAD v3: 10-70435554-C-T
gnomAD v4: 10-70435554-C-T
MyVariant Identifiers: chr10:g.72195310C>T (hg19) chr10:g.70435554C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435554C>T , CM000672.2:g.70435554C>T GRCh38
NC_000010.10:g.72195310C>T , CM000672.1:g.72195310C>T GRCh37
NC_000010.9:g.71865316C>T NCBI36
NG_012448.1:g.11156G>A
NG_012448.2:g.17395G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.623G>A MANE Select ENSP00000287139.3:p.Gly208Asp
ENST00000287139.7:c.623G>A ENSP00000287139.3:p.Gly208Asp
ENST00000414871.1:c.458G>A ENSP00000394468.1:p.Gly153Asp
NM_018055.4:c.623G>A NP_060525.3:p.Gly208Asp
NM_001329906.1:c.224G>A NP_001316835.1:p.Gly75Asp
XM_024448028.1:c.224G>A XP_024303796.1:p.Gly75Asp
NM_018055.5:c.623G>A MANE Select NP_060525.3:p.Gly208Asp
NM_001329906.2:c.224G>A NP_001316835.1:p.Gly75Asp
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