Canonical Allele Identifier: CA2184234625
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781005A= , CM000677.2:g.66781005A= GRCh38
NC_000015.9:g.67073343A= , CM000677.1:g.67073343A= GRCh37
NC_000015.8:g.64860397A= NCBI36
NG_012244.1:g.83670A=
NG_012244.2:g.83670A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.961A= MANE Select ENSP00000288840.5:p.Met321=
ENST00000288840.9:c.961A= ENSP00000288840.5:p.Met321=
ENST00000557916.5:c.1093A= ENSP00000452955.1:n.1093A=
ENST00000559931.5:c.265A= ENSP00000453446.1:n.265A=
NM_005585.4:c.961A= NP_005576.3:p.Met321=
NR_027654.1:n.2016A=
XM_011521561.1:c.178A= XP_011519863.1:p.Met60=
XR_931825.1:n.2360A=
XM_011521561.2:c.178A= XP_011519863.1:p.Met60=
NM_005585.5:c.961A= MANE Select NP_005576.3:p.Met321=
NR_027654.2:n.2116A=