Canonical Allele Identifier: CA470279576
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs1589152337
MyVariant Identifiers: chr10:g.72195309A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435553A>C , CM000672.2:g.70435553A>C GRCh38
NC_000010.10:g.72195309A>C , CM000672.1:g.72195309A>C GRCh37
NC_000010.9:g.71865315A>C NCBI36
NG_012448.1:g.11157T>G
NG_012448.2:g.17396T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.624T>G MANE Select ENSP00000287139.3:p.Gly208=
ENST00000287139.7:c.624T>G ENSP00000287139.3:p.Gly208=
ENST00000414871.1:c.459T>G ENSP00000394468.1:p.Gly153=
NM_018055.4:c.624T>G NP_060525.3:p.Gly208=
NM_001329906.1:c.225T>G NP_001316835.1:p.Gly75=
XM_024448028.1:c.225T>G XP_024303796.1:p.Gly75=
NM_018055.5:c.624T>G MANE Select NP_060525.3:p.Gly208=
NM_001329906.2:c.225T>G NP_001316835.1:p.Gly75=