Canonical Allele Identifier: CA392948253
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1893015835

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703269C>T , CM000677.2:g.66703269C>T GRCh38
NC_000015.9:g.66995607C>T , CM000677.1:g.66995607C>T GRCh37
NC_000015.8:g.64782661C>T NCBI36
NG_012244.1:g.5934C>T
NG_012244.2:g.5934C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.11C>T MANE Select ENSP00000288840.5:p.Ser4Phe
ENST00000288840.9:c.11C>T ENSP00000288840.5:p.Ser4Phe
ENST00000557916.5:c.11C>T ENSP00000452955.1:p.Ser4Phe
ENST00000612349.1:n.193C>T
NM_005585.4:c.11C>T NP_005576.3:p.Ser4Phe
NR_027654.1:n.934C>T
XR_931825.1:n.1170C>T
XR_931826.1:n.1170C>T
XR_931827.1:n.1170C>T
XR_931827.2:n.1160C>T
NM_005585.5:c.11C>T MANE Select NP_005576.3:p.Ser4Phe
NR_027654.2:n.1034C>T