Canonical Allele Identifier: CA2629100850
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703213A>G , CM000677.2:g.66703213A>G GRCh38
NC_000015.9:g.66995551A>G , CM000677.1:g.66995551A>G GRCh37
NC_000015.8:g.64782605A>G NCBI36
NG_012244.1:g.5878A>G
NG_012244.2:g.5878A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.-46A>G MANE Select ENSP00000288840.5:n.-46A>G
ENST00000288840.9:c.-46A>G ENSP00000288840.5:n.-46A>G
ENST00000612349.1:n.137A>G
NM_005585.4:c.-46A>G NP_005576.3:n.-46A>G
NR_027654.1:n.878A>G
XR_931825.1:n.1114A>G
XR_931826.1:n.1114A>G
XR_931827.1:n.1114A>G
XR_931827.2:n.1104A>G
NM_005585.5:c.-46A>G MANE Select NP_005576.3:n.-46A>G
NR_027654.2:n.978A>G