Canonical Allele Identifier: CA470279564
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195303G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435547G>T , CM000672.2:g.70435547G>T GRCh38
NC_000010.10:g.72195303G>T , CM000672.1:g.72195303G>T GRCh37
NC_000010.9:g.71865309G>T NCBI36
NG_012448.1:g.11163C>A
NG_012448.2:g.17402C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.630C>A MANE Select ENSP00000287139.3:p.Ser210=
ENST00000287139.7:c.630C>A ENSP00000287139.3:p.Ser210=
ENST00000414871.1:c.465C>A ENSP00000394468.1:p.Ser155=
NM_018055.4:c.630C>A NP_060525.3:p.Ser210=
NM_001329906.1:c.231C>A NP_001316835.1:p.Ser77=
XM_024448028.1:c.231C>A XP_024303796.1:p.Ser77=
NM_018055.5:c.630C>A MANE Select NP_060525.3:p.Ser210=
NM_001329906.2:c.231C>A NP_001316835.1:p.Ser77=