Canonical Allele Identifier: CA2629105665
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66780900G>C , CM000677.2:g.66780900G>C GRCh38
NC_000015.9:g.67073238G>C , CM000677.1:g.67073238G>C GRCh37
NC_000015.8:g.64860292G>C NCBI36
NG_012244.1:g.83565G>C
NG_012244.2:g.83565G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.953-97G>C MANE Select ENSP00000288840.5:n.953-97G>C
ENST00000288840.9:c.953-97G>C ENSP00000288840.5:n.953-97G>C
ENST00000557916.5:c.1085-97G>C ENSP00000452955.1:n.1085-97G>C
ENST00000559931.5:c.257-97G>C ENSP00000453446.1:n.257-97G>C
NM_005585.4:c.953-97G>C NP_005576.3:n.953-97G>C
NR_027654.1:n.2008-97G>C
XM_011521561.1:c.170-97G>C XP_011519863.1:n.170-97G>C
XR_931825.1:n.2352-97G>C
XM_011521561.2:c.170-97G>C XP_011519863.1:n.170-97G>C
NM_005585.5:c.953-97G>C MANE Select NP_005576.3:n.953-97G>C
NR_027654.2:n.2108-97G>C