Canonical Allele Identifier: CA392948208
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703259A>T , CM000677.2:g.66703259A>T GRCh38
NC_000015.9:g.66995597A>T , CM000677.1:g.66995597A>T GRCh37
NC_000015.8:g.64782651A>T NCBI36
NG_012244.1:g.5924A>T
NG_012244.2:g.5924A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288840.10:c.1A>T MANE Select ENSP00000288840.5:p.Met1Leu
ENST00000288840.9:c.1A>T ENSP00000288840.5:p.Met1Leu
ENST00000557916.5:c.1A>T ENSP00000452955.1:p.Met1Leu
ENST00000612349.1:n.183A>T
NM_005585.4:c.1A>T NP_005576.3:p.Met1Leu
NR_027654.1:n.924A>T
XR_931825.1:n.1160A>T
XR_931826.1:n.1160A>T
XR_931827.1:n.1160A>T
XR_931827.2:n.1150A>T
NM_005585.5:c.1A>T MANE Select NP_005576.3:p.Met1Leu
NR_027654.2:n.1024A>T