Canonical Allele Identifier: CA393201620

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073370C>T (hg19) ; chr15:g.66781032C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781032C>T , CM000677.2:g.66781032C>T	GRCh38
NC_000015.9:g.67073370C>T , CM000677.1:g.67073370C>T	GRCh37
NC_000015.8:g.64860424C>T	NCBI36
NG_012244.1:g.83697C>T
NG_012244.2:g.83697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.988C>T MANE Select	ENSP00000288840.5:p.His330Tyr
ENST00000288840.9:c.988C>T	ENSP00000288840.5:p.His330Tyr
ENST00000557916.5:c.1120C>T	ENSP00000452955.1:n.1120C>T
ENST00000559931.5:c.292C>T	ENSP00000453446.1:n.292C>T
NM_005585.4:c.988C>T	NP_005576.3:p.His330Tyr
NR_027654.1:n.2043C>T
XM_011521561.1:c.205C>T	XP_011519863.1:p.His69Tyr
XR_931825.1:n.2387C>T
XM_011521561.2:c.205C>T	XP_011519863.1:p.His69Tyr
NM_005585.5:c.988C>T MANE Select	NP_005576.3:p.His330Tyr
NR_027654.2:n.2143C>T