Canonical Allele Identifier: CA209321822

Gene: NODAL

Linked Data

• dbSNP Id: rs907057720
• gnomAD v3: 10-70435644-C-A
• gnomAD v4: 10-70435644-C-A
• MyVariant Identifiers: chr10:g.72195400C>A (hg19) ; chr10:g.70435644C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435644C>A , CM000672.2:g.70435644C>A	GRCh38
NC_000010.10:g.72195400C>A , CM000672.1:g.72195400C>A	GRCh37
NC_000010.9:g.71865406C>A	NCBI36
NG_012448.1:g.11066G>T
NG_012448.2:g.17305G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.533G>T MANE Select	ENSP00000287139.3:p.Gly178Val
ENST00000287139.7:c.533G>T	ENSP00000287139.3:p.Gly178Val
ENST00000414871.1:c.368G>T	ENSP00000394468.1:p.Gly123Val
NM_018055.4:c.533G>T	NP_060525.3:p.Gly178Val
NM_001329906.1:c.134G>T	NP_001316835.1:p.Gly45Val
XM_024448028.1:c.134G>T	XP_024303796.1:p.Gly45Val
NM_018055.5:c.533G>T MANE Select	NP_060525.3:p.Gly178Val
NM_001329906.2:c.134G>T	NP_001316835.1:p.Gly45Val