Canonical Allele Identifier: CA490908887

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781034-C-T
• MyVariant Identifiers: chr15:g.67073372C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781034C>T , CM000677.2:g.66781034C>T	GRCh38
NC_000015.9:g.67073372C>T , CM000677.1:g.67073372C>T	GRCh37
NC_000015.8:g.64860426C>T	NCBI36
NG_012244.1:g.83699C>T
NG_012244.2:g.83699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.990C>T MANE Select	ENSP00000288840.5:p.His330=
ENST00000288840.9:c.990C>T	ENSP00000288840.5:p.His330=
ENST00000557916.5:c.1122C>T	ENSP00000452955.1:n.1122C>T
ENST00000559931.5:c.294C>T	ENSP00000453446.1:n.294C>T
NM_005585.4:c.990C>T	NP_005576.3:p.His330=
NR_027654.1:n.2045C>T
XM_011521561.1:c.207C>T	XP_011519863.1:p.His69=
XR_931825.1:n.2389C>T
XM_011521561.2:c.207C>T	XP_011519863.1:p.His69=
NM_005585.5:c.990C>T MANE Select	NP_005576.3:p.His330=
NR_027654.2:n.2145C>T