Canonical Allele Identifier: CA7626697

Gene: SMAD6

Linked Data

• dbSNP Id: rs201517247
• ExAC: 15:67073345 G / A
• gnomAD v2: 15-67073345-G-A
• gnomAD v3: 15-66781007-G-A
• gnomAD v4: 15-66781007-G-A
• MyVariant Identifiers: chr15:g.67073345G>A (hg19) ; chr15:g.66781007G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781007G>A , CM000677.2:g.66781007G>A	GRCh38
NC_000015.9:g.67073345G>A , CM000677.1:g.67073345G>A	GRCh37
NC_000015.8:g.64860399G>A	NCBI36
NG_012244.1:g.83672G>A
NG_012244.2:g.83672G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.963G>A MANE Select	ENSP00000288840.5:p.Met321Ile
ENST00000288840.9:c.963G>A	ENSP00000288840.5:p.Met321Ile
ENST00000557916.5:c.1095G>A	ENSP00000452955.1:n.1095G>A
ENST00000559931.5:c.267G>A	ENSP00000453446.1:n.267G>A
NM_005585.4:c.963G>A	NP_005576.3:p.Met321Ile
NR_027654.1:n.2018G>A
XM_011521561.1:c.180G>A	XP_011519863.1:p.Met60Ile
XR_931825.1:n.2362G>A
XM_011521561.2:c.180G>A	XP_011519863.1:p.Met60Ile
NM_005585.5:c.963G>A MANE Select	NP_005576.3:p.Met321Ile
NR_027654.2:n.2118G>A