Canonical Allele Identifier: CA2609510330
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432209-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432209T>G , CM000672.2:g.70432209T>G GRCh38
NC_000010.10:g.72191965T>G , CM000672.1:g.72191965T>G GRCh37
NC_000010.9:g.71861971T>G NCBI36
NG_012448.1:g.14501A>C
NG_012448.2:g.20740A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*727A>C MANE Select ENSP00000287139.3:n.*727A>C
NM_018055.4:c.*727A>C NP_060525.3:n.*727A>C
NM_001329906.1:c.*727A>C NP_001316835.1:n.*727A>C
NM_018055.5:c.*727A>C MANE Select NP_060525.3:n.*727A>C
NM_001329906.2:c.*727A>C NP_001316835.1:n.*727A>C
Search 100 bp 5'
Search 100 bp 3'