Canonical Allele Identifier: CA470278903
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs1845339142
MyVariant Identifiers: chr10:g.72195399T>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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