Canonical Allele Identifier: CA393201623
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781033A>T , CM000677.2:g.66781033A>T GRCh38
NC_000015.9:g.67073371A>T , CM000677.1:g.67073371A>T GRCh37
NC_000015.8:g.64860425A>T NCBI36
NG_012244.1:g.83698A>T
NG_012244.2:g.83698A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.989A>T MANE Select ENSP00000288840.5:p.His330Leu
ENST00000288840.9:c.989A>T ENSP00000288840.5:p.His330Leu
ENST00000557916.5:c.1121A>T ENSP00000452955.1:n.1121A>T
ENST00000559931.5:c.293A>T ENSP00000453446.1:n.293A>T
NM_005585.4:c.989A>T NP_005576.3:p.His330Leu
NR_027654.1:n.2044A>T
XM_011521561.1:c.206A>T XP_011519863.1:p.His69Leu
XR_931825.1:n.2388A>T
XM_011521561.2:c.206A>T XP_011519863.1:p.His69Leu
NM_005585.5:c.989A>T MANE Select NP_005576.3:p.His330Leu
NR_027654.2:n.2144A>T