Canonical Allele Identifier: CA1918248408
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs1196418389

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432206G>A , CM000672.2:g.70432206G>A GRCh38
NC_000010.10:g.72191962G>A , CM000672.1:g.72191962G>A GRCh37
NC_000010.9:g.71861968G>A NCBI36
NG_012448.1:g.14504C>T
NG_012448.2:g.20743C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*730C>T MANE Select ENSP00000287139.3:n.*730C>T
NM_018055.4:c.*730C>T NP_060525.3:n.*730C>T
NM_001329906.1:c.*730C>T NP_001316835.1:n.*730C>T
NM_018055.5:c.*730C>T MANE Select NP_060525.3:n.*730C>T
NM_001329906.2:c.*730C>T NP_001316835.1:n.*730C>T