Canonical Allele Identifier: CA470279553
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs922821850
MyVariant Identifiers: chr10:g.72195300G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435544G>C , CM000672.2:g.70435544G>C GRCh38
NC_000010.10:g.72195300G>C , CM000672.1:g.72195300G>C GRCh37
NC_000010.9:g.71865306G>C NCBI36
NG_012448.1:g.11166C>G
NG_012448.2:g.17405C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.633C>G MANE Select ENSP00000287139.3:p.Thr211=
ENST00000287139.7:c.633C>G ENSP00000287139.3:p.Thr211=
ENST00000414871.1:c.468C>G ENSP00000394468.1:p.Thr156=
NM_018055.4:c.633C>G NP_060525.3:p.Thr211=
NM_001329906.1:c.234C>G NP_001316835.1:p.Thr78=
XM_024448028.1:c.234C>G XP_024303796.1:p.Thr78=
NM_018055.5:c.633C>G MANE Select NP_060525.3:p.Thr211=
NM_001329906.2:c.234C>G NP_001316835.1:p.Thr78=
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