Canonical Allele Identifier: CA393201574
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781011C>G , CM000677.2:g.66781011C>G GRCh38
NC_000015.9:g.67073349C>G , CM000677.1:g.67073349C>G GRCh37
NC_000015.8:g.64860403C>G NCBI36
NG_012244.1:g.83676C>G
NG_012244.2:g.83676C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.967C>G MANE Select ENSP00000288840.5:p.Pro323Ala
ENST00000288840.9:c.967C>G ENSP00000288840.5:p.Pro323Ala
ENST00000557916.5:c.1099C>G ENSP00000452955.1:n.1099C>G
ENST00000559931.5:c.271C>G ENSP00000453446.1:n.271C>G
NM_005585.4:c.967C>G NP_005576.3:p.Pro323Ala
NR_027654.1:n.2022C>G
XM_011521561.1:c.184C>G XP_011519863.1:p.Pro62Ala
XR_931825.1:n.2366C>G
XM_011521561.2:c.184C>G XP_011519863.1:p.Pro62Ala
NM_005585.5:c.967C>G MANE Select NP_005576.3:p.Pro323Ala
NR_027654.2:n.2122C>G