Canonical Allele Identifier: CA470279562
Gene: NODAL HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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