Canonical Allele Identifier: CA393201550

Gene: SMAD6

Linked Data

• dbSNP Id: rs148705603
• MyVariant Identifiers: chr15:g.67073338C>G (hg19) ; chr15:g.66781000C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781000C>G , CM000677.2:g.66781000C>G	GRCh38
NC_000015.9:g.67073338C>G , CM000677.1:g.67073338C>G	GRCh37
NC_000015.8:g.64860392C>G	NCBI36
NG_012244.1:g.83665C>G
NG_012244.2:g.83665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.956C>G MANE Select	ENSP00000288840.5:p.Ala319Gly
ENST00000288840.9:c.956C>G	ENSP00000288840.5:p.Ala319Gly
ENST00000557916.5:c.1088C>G	ENSP00000452955.1:n.1088C>G
ENST00000559931.5:c.260C>G	ENSP00000453446.1:n.260C>G
NM_005585.4:c.956C>G	NP_005576.3:p.Ala319Gly
NR_027654.1:n.2011C>G
XM_011521561.1:c.173C>G	XP_011519863.1:p.Ala58Gly
XR_931825.1:n.2355C>G
XM_011521561.2:c.173C>G	XP_011519863.1:p.Ala58Gly
NM_005585.5:c.956C>G MANE Select	NP_005576.3:p.Ala319Gly
NR_027654.2:n.2111C>G