Canonical Allele Identifier: CA2609510329
Gene: NODAL HGNC NCBI

Linked Data

gnomAD v4: 10-70432208-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432208G>T , CM000672.2:g.70432208G>T GRCh38
NC_000010.10:g.72191964G>T , CM000672.1:g.72191964G>T GRCh37
NC_000010.9:g.71861970G>T NCBI36
NG_012448.1:g.14502C>A
NG_012448.2:g.20741C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*728C>A MANE Select ENSP00000287139.3:n.*728C>A
NM_018055.4:c.*728C>A NP_060525.3:n.*728C>A
NM_001329906.1:c.*728C>A NP_001316835.1:n.*728C>A
NM_018055.5:c.*728C>A MANE Select NP_060525.3:n.*728C>A
NM_001329906.2:c.*728C>A NP_001316835.1:n.*728C>A
Search 100 bp 5'
Search 100 bp 3'