Canonical Allele Identifier: CA393201806
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781119G>A , CM000677.2:g.66781119G>A GRCh38
NC_000015.9:g.67073457G>A , CM000677.1:g.67073457G>A GRCh37
NC_000015.8:g.64860511G>A NCBI36
NG_012244.1:g.83784G>A
NG_012244.2:g.83784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1075G>A MANE Select ENSP00000288840.5:p.Asp359Asn
ENST00000288840.9:c.1075G>A ENSP00000288840.5:p.Asp359Asn
ENST00000557916.5:c.1207G>A ENSP00000452955.1:n.1207G>A
ENST00000559931.5:c.379G>A ENSP00000453446.1:n.379G>A
NM_005585.4:c.1075G>A NP_005576.3:p.Asp359Asn
NR_027654.1:n.2130G>A
XM_011521561.1:c.292G>A XP_011519863.1:p.Asp98Asn
XR_931825.1:n.2474G>A
XM_011521561.2:c.292G>A XP_011519863.1:p.Asp98Asn
NM_005585.5:c.1075G>A MANE Select NP_005576.3:p.Asp359Asn
NR_027654.2:n.2230G>A