Canonical Allele Identifier: CA470279572
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195306C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435550C>G , CM000672.2:g.70435550C>G GRCh38
NC_000010.10:g.72195306C>G , CM000672.1:g.72195306C>G GRCh37
NC_000010.9:g.71865312C>G NCBI36
NG_012448.1:g.11160G>C
NG_012448.2:g.17399G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.627G>C MANE Select ENSP00000287139.3:p.Gly209=
ENST00000287139.7:c.627G>C ENSP00000287139.3:p.Gly209=
ENST00000414871.1:c.462G>C ENSP00000394468.1:p.Gly154=
NM_018055.4:c.627G>C NP_060525.3:p.Gly209=
NM_001329906.1:c.228G>C NP_001316835.1:p.Gly76=
XM_024448028.1:c.228G>C XP_024303796.1:p.Gly76=
NM_018055.5:c.627G>C MANE Select NP_060525.3:p.Gly209=
NM_001329906.2:c.228G>C NP_001316835.1:p.Gly76=
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