Canonical Allele Identifier: CA393201683
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1444388251

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781059C>G , CM000677.2:g.66781059C>G GRCh38
NC_000015.9:g.67073397C>G , CM000677.1:g.67073397C>G GRCh37
NC_000015.8:g.64860451C>G NCBI36
NG_012244.1:g.83724C>G
NG_012244.2:g.83724C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1015C>G MANE Select ENSP00000288840.5:p.His339Asp
ENST00000288840.9:c.1015C>G ENSP00000288840.5:p.His339Asp
ENST00000557916.5:c.1147C>G ENSP00000452955.1:n.1147C>G
ENST00000559931.5:c.319C>G ENSP00000453446.1:n.319C>G
NM_005585.4:c.1015C>G NP_005576.3:p.His339Asp
NR_027654.1:n.2070C>G
XM_011521561.1:c.232C>G XP_011519863.1:p.His78Asp
XR_931825.1:n.2414C>G
XM_011521561.2:c.232C>G XP_011519863.1:p.His78Asp
NM_005585.5:c.1015C>G MANE Select NP_005576.3:p.His339Asp
NR_027654.2:n.2170C>G