Canonical Allele Identifier: CA470279280
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195204T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435448T>C , CM000672.2:g.70435448T>C GRCh38
NC_000010.10:g.72195204T>C , CM000672.1:g.72195204T>C GRCh37
NC_000010.9:g.71865210T>C NCBI36
NG_012448.1:g.11262A>G
NG_012448.2:g.17501A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.729A>G MANE Select ENSP00000287139.3:p.Arg243=
ENST00000287139.7:c.729A>G ENSP00000287139.3:p.Arg243=
ENST00000414871.1:c.564A>G ENSP00000394468.1:p.Arg188=
NM_018055.4:c.729A>G NP_060525.3:p.Arg243=
NM_001329906.1:c.330A>G NP_001316835.1:p.Arg110=
XM_024448028.1:c.330A>G XP_024303796.1:p.Arg110=
NM_018055.5:c.729A>G MANE Select NP_060525.3:p.Arg243=
NM_001329906.2:c.330A>G NP_001316835.1:p.Arg110=