Canonical Allele Identifier: CA392948280
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703277T>G , CM000677.2:g.66703277T>G GRCh38
NC_000015.9:g.66995615T>G , CM000677.1:g.66995615T>G GRCh37
NC_000015.8:g.64782669T>G NCBI36
NG_012244.1:g.5942T>G
NG_012244.2:g.5942T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.19T>G MANE Select ENSP00000288840.5:p.Ser7Ala
ENST00000288840.9:c.19T>G ENSP00000288840.5:p.Ser7Ala
ENST00000557916.5:c.19T>G ENSP00000452955.1:p.Ser7Ala
ENST00000612349.1:n.201T>G
NM_005585.4:c.19T>G NP_005576.3:p.Ser7Ala
NR_027654.1:n.942T>G
XR_931825.1:n.1178T>G
XR_931826.1:n.1178T>G
XR_931827.1:n.1178T>G
XR_931827.2:n.1168T>G
NM_005585.5:c.19T>G MANE Select NP_005576.3:p.Ser7Ala
NR_027654.2:n.1042T>G