Canonical Allele Identifier: CA392948417
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703320A>G , CM000677.2:g.66703320A>G GRCh38
NC_000015.9:g.66995658A>G , CM000677.1:g.66995658A>G GRCh37
NC_000015.8:g.64782712A>G NCBI36
NG_012244.1:g.5985A>G
NG_012244.2:g.5985A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.62A>G MANE Select ENSP00000288840.5:p.Asp21Gly
ENST00000288840.9:c.62A>G ENSP00000288840.5:p.Asp21Gly
ENST00000557916.5:c.62A>G ENSP00000452955.1:p.Asp21Gly
ENST00000612349.1:n.244A>G
NM_005585.4:c.62A>G NP_005576.3:p.Asp21Gly
NR_027654.1:n.985A>G
XR_931825.1:n.1221A>G
XR_931826.1:n.1221A>G
XR_931827.1:n.1221A>G
XR_931827.2:n.1211A>G
NM_005585.5:c.62A>G MANE Select NP_005576.3:p.Asp21Gly
NR_027654.2:n.1085A>G