Canonical Allele Identifier: CA393201567

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073346T>A (hg19) ; chr15:g.66781008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781008T>A , CM000677.2:g.66781008T>A	GRCh38
NC_000015.9:g.67073346T>A , CM000677.1:g.67073346T>A	GRCh37
NC_000015.8:g.64860400T>A	NCBI36
NG_012244.1:g.83673T>A
NG_012244.2:g.83673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.964T>A MANE Select	ENSP00000288840.5:p.Ser322Thr
ENST00000288840.9:c.964T>A	ENSP00000288840.5:p.Ser322Thr
ENST00000557916.5:c.1096T>A	ENSP00000452955.1:n.1096T>A
ENST00000559931.5:c.268T>A	ENSP00000453446.1:n.268T>A
NM_005585.4:c.964T>A	NP_005576.3:p.Ser322Thr
NR_027654.1:n.2019T>A
XM_011521561.1:c.181T>A	XP_011519863.1:p.Ser61Thr
XR_931825.1:n.2363T>A
XM_011521561.2:c.181T>A	XP_011519863.1:p.Ser61Thr
NM_005585.5:c.964T>A MANE Select	NP_005576.3:p.Ser322Thr
NR_027654.2:n.2119T>A