Canonical Allele Identifier: CA470279274
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195201A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435445A>G , CM000672.2:g.70435445A>G GRCh38
NC_000010.10:g.72195201A>G , CM000672.1:g.72195201A>G GRCh37
NC_000010.9:g.71865207A>G NCBI36
NG_012448.1:g.11265T>C
NG_012448.2:g.17504T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.732T>C MANE Select ENSP00000287139.3:p.Ser244=
ENST00000287139.7:c.732T>C ENSP00000287139.3:p.Ser244=
ENST00000414871.1:c.567T>C ENSP00000394468.1:p.Ser189=
NM_018055.4:c.732T>C NP_060525.3:p.Ser244=
NM_001329906.1:c.333T>C NP_001316835.1:p.Ser111=
XM_024448028.1:c.333T>C XP_024303796.1:p.Ser111=
NM_018055.5:c.732T>C MANE Select NP_060525.3:p.Ser244=
NM_001329906.2:c.333T>C NP_001316835.1:p.Ser111=