Canonical Allele Identifier: CA2184231510
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs967114113

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66774173C>G , CM000677.2:g.66774173C>G GRCh38
NC_000015.9:g.67066511C>G , CM000677.1:g.67066511C>G GRCh37
NC_000015.8:g.64853565C>G NCBI36
NG_012244.1:g.76838C>G
NG_012244.2:g.76838C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000288840.10:c.953-6824C>G MANE Select ENSP00000288840.5:n.953-6824C>G
ENST00000288840.9:c.953-6824C>G ENSP00000288840.5:n.953-6824C>G
ENST00000557916.5:c.1085-6824C>G ENSP00000452955.1:n.1085-6824C>G
ENST00000559931.5:c.257-6824C>G ENSP00000453446.1:n.257-6824C>G
NM_005585.4:c.953-6824C>G NP_005576.3:n.953-6824C>G
NR_027654.1:n.2008-6824C>G
XM_011521561.1:c.170-6824C>G XP_011519863.1:n.170-6824C>G
XR_931825.1:n.2352-6824C>G
XM_011521561.2:c.170-6824C>G XP_011519863.1:n.170-6824C>G
NM_005585.5:c.953-6824C>G MANE Select NP_005576.3:n.953-6824C>G
NR_027654.2:n.2108-6824C>G