Canonical Allele Identifier: CA470278902
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195399T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435643T>A , CM000672.2:g.70435643T>A GRCh38
NC_000010.10:g.72195399T>A , CM000672.1:g.72195399T>A GRCh37
NC_000010.9:g.71865405T>A NCBI36
NG_012448.1:g.11067A>T
NG_012448.2:g.17306A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.534A>T MANE Select ENSP00000287139.3:p.Gly178=
ENST00000287139.7:c.534A>T ENSP00000287139.3:p.Gly178=
ENST00000414871.1:c.369A>T ENSP00000394468.1:p.Gly123=
NM_018055.4:c.534A>T NP_060525.3:p.Gly178=
NM_001329906.1:c.135A>T NP_001316835.1:p.Gly45=
XM_024448028.1:c.135A>T XP_024303796.1:p.Gly45=
NM_018055.5:c.534A>T MANE Select NP_060525.3:p.Gly178=
NM_001329906.2:c.135A>T NP_001316835.1:p.Gly45=