Canonical Allele Identifier: CA470279290
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195206T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435450T>G , CM000672.2:g.70435450T>G GRCh38
NC_000010.10:g.72195206T>G , CM000672.1:g.72195206T>G GRCh37
NC_000010.9:g.71865212T>G NCBI36
NG_012448.1:g.11260A>C
NG_012448.2:g.17499A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.727A>C MANE Select ENSP00000287139.3:p.Arg243=
ENST00000287139.7:c.727A>C ENSP00000287139.3:p.Arg243=
ENST00000414871.1:c.562A>C ENSP00000394468.1:p.Arg188=
NM_018055.4:c.727A>C NP_060525.3:p.Arg243=
NM_001329906.1:c.328A>C NP_001316835.1:p.Arg110=
XM_024448028.1:c.328A>C XP_024303796.1:p.Arg110=
NM_018055.5:c.727A>C MANE Select NP_060525.3:p.Arg243=
NM_001329906.2:c.328A>C NP_001316835.1:p.Arg110=