Canonical Allele Identifier: CA667995039

Gene: NODAL

Linked Data

• dbSNP Id: rs1405253495
• gnomAD v3: 10-70435263-C-T
• gnomAD v4: 10-70435263-C-T
• MyVariant Identifiers: chr10:g.72195019C>T (hg19) ; chr10:g.70435263C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435263C>T , CM000672.2:g.70435263C>T	GRCh38
NC_000010.10:g.72195019C>T , CM000672.1:g.72195019C>T	GRCh37
NC_000010.9:g.71865025C>T	NCBI36
NG_012448.1:g.11447G>A
NG_012448.2:g.17686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.891+23G>A MANE Select	ENSP00000287139.3:n.891+23G>A
ENST00000287139.7:c.891+23G>A	ENSP00000287139.3:n.891+23G>A
ENST00000414871.1:c.726+23G>A	ENSP00000394468.1:n.726+23G>A
NM_018055.4:c.891+23G>A	NP_060525.3:n.891+23G>A
NM_001329906.1:c.492+23G>A	NP_001316835.1:n.492+23G>A
XM_024448028.1:c.492+23G>A	XP_024303796.1:n.492+23G>A
NM_018055.5:c.891+23G>A MANE Select	NP_060525.3:n.891+23G>A
NM_001329906.2:c.492+23G>A	NP_001316835.1:n.492+23G>A