Canonical Allele Identifier: CA393201651

Gene: SMAD6

Linked Data

• dbSNP Id: rs1275289201
• MyVariant Identifiers: chr15:g.67073383T>C (hg19) ; chr15:g.66781045T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781045T>C , CM000677.2:g.66781045T>C	GRCh38
NC_000015.9:g.67073383T>C , CM000677.1:g.67073383T>C	GRCh37
NC_000015.8:g.64860437T>C	NCBI36
NG_012244.1:g.83710T>C
NG_012244.2:g.83710T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1001T>C MANE Select	ENSP00000288840.5:p.Val334Ala
ENST00000288840.9:c.1001T>C	ENSP00000288840.5:p.Val334Ala
ENST00000557916.5:c.1133T>C	ENSP00000452955.1:n.1133T>C
ENST00000559931.5:c.305T>C	ENSP00000453446.1:n.305T>C
NM_005585.4:c.1001T>C	NP_005576.3:p.Val334Ala
NR_027654.1:n.2056T>C
XM_011521561.1:c.218T>C	XP_011519863.1:p.Val73Ala
XR_931825.1:n.2400T>C
XM_011521561.2:c.218T>C	XP_011519863.1:p.Val73Ala
NM_005585.5:c.1001T>C MANE Select	NP_005576.3:p.Val334Ala
NR_027654.2:n.2156T>C