Canonical Allele Identifier: CA490909023

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073471C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781133C>G , CM000677.2:g.66781133C>G	GRCh38
NC_000015.9:g.67073471C>G , CM000677.1:g.67073471C>G	GRCh37
NC_000015.8:g.64860525C>G	NCBI36
NG_012244.1:g.83798C>G
NG_012244.2:g.83798C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1089C>G MANE Select	ENSP00000288840.5:p.Gly363=
ENST00000288840.9:c.1089C>G	ENSP00000288840.5:p.Gly363=
ENST00000557916.5:c.1221C>G	ENSP00000452955.1:n.1221C>G
ENST00000559931.5:c.393C>G	ENSP00000453446.1:n.393C>G
NM_005585.4:c.1089C>G	NP_005576.3:p.Gly363=
NR_027654.1:n.2144C>G
XM_011521561.1:c.306C>G	XP_011519863.1:p.Gly102=
XR_931825.1:n.2488C>G
XM_011521561.2:c.306C>G	XP_011519863.1:p.Gly102=
NM_005585.5:c.1089C>G MANE Select	NP_005576.3:p.Gly363=
NR_027654.2:n.2244C>G