Canonical Allele Identifier: CA393201572
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781009C>G , CM000677.2:g.66781009C>G GRCh38
NC_000015.9:g.67073347C>G , CM000677.1:g.67073347C>G GRCh37
NC_000015.8:g.64860401C>G NCBI36
NG_012244.1:g.83674C>G
NG_012244.2:g.83674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.965C>G MANE Select ENSP00000288840.5:p.Ser322Cys
ENST00000288840.9:c.965C>G ENSP00000288840.5:p.Ser322Cys
ENST00000557916.5:c.1097C>G ENSP00000452955.1:n.1097C>G
ENST00000559931.5:c.269C>G ENSP00000453446.1:n.269C>G
NM_005585.4:c.965C>G NP_005576.3:p.Ser322Cys
NR_027654.1:n.2020C>G
XM_011521561.1:c.182C>G XP_011519863.1:p.Ser61Cys
XR_931825.1:n.2364C>G
XM_011521561.2:c.182C>G XP_011519863.1:p.Ser61Cys
NM_005585.5:c.965C>G MANE Select NP_005576.3:p.Ser322Cys
NR_027654.2:n.2120C>G