Canonical Allele Identifier: CA490908873

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781022-C-T
• MyVariant Identifiers: chr15:g.67073360C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781022C>T , CM000677.2:g.66781022C>T	GRCh38
NC_000015.9:g.67073360C>T , CM000677.1:g.67073360C>T	GRCh37
NC_000015.8:g.64860414C>T	NCBI36
NG_012244.1:g.83687C>T
NG_012244.2:g.83687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.978C>T MANE Select	ENSP00000288840.5:p.Thr326=
ENST00000288840.9:c.978C>T	ENSP00000288840.5:p.Thr326=
ENST00000557916.5:c.1110C>T	ENSP00000452955.1:n.1110C>T
ENST00000559931.5:c.282C>T	ENSP00000453446.1:n.282C>T
NM_005585.4:c.978C>T	NP_005576.3:p.Thr326=
NR_027654.1:n.2033C>T
XM_011521561.1:c.195C>T	XP_011519863.1:p.Thr65=
XR_931825.1:n.2377C>T
XM_011521561.2:c.195C>T	XP_011519863.1:p.Thr65=
NM_005585.5:c.978C>T MANE Select	NP_005576.3:p.Thr326=
NR_027654.2:n.2133C>T