Canonical Allele Identifier: CA470279292
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs1845333111
MyVariant Identifiers: chr10:g.72195207G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435451G>A , CM000672.2:g.70435451G>A GRCh38
NC_000010.10:g.72195207G>A , CM000672.1:g.72195207G>A GRCh37
NC_000010.9:g.71865213G>A NCBI36
NG_012448.1:g.11259C>T
NG_012448.2:g.17498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.726C>T MANE Select ENSP00000287139.3:p.Asp242=
ENST00000287139.7:c.726C>T ENSP00000287139.3:p.Asp242=
ENST00000414871.1:c.561C>T ENSP00000394468.1:p.Asp187=
NM_018055.4:c.726C>T NP_060525.3:p.Asp242=
NM_001329906.1:c.327C>T NP_001316835.1:p.Asp109=
XM_024448028.1:c.327C>T XP_024303796.1:p.Asp109=
NM_018055.5:c.726C>T MANE Select NP_060525.3:p.Asp242=
NM_001329906.2:c.327C>T NP_001316835.1:p.Asp109=