Canonical Allele Identifier: CA393201607

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781026-C-T
• MyVariant Identifiers: chr15:g.67073364C>T (hg19) ; chr15:g.66781026C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781026C>T , CM000677.2:g.66781026C>T	GRCh38
NC_000015.9:g.67073364C>T , CM000677.1:g.67073364C>T	GRCh37
NC_000015.8:g.64860418C>T	NCBI36
NG_012244.1:g.83691C>T
NG_012244.2:g.83691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.982C>T MANE Select	ENSP00000288840.5:p.Pro328Ser
ENST00000288840.9:c.982C>T	ENSP00000288840.5:p.Pro328Ser
ENST00000557916.5:c.1114C>T	ENSP00000452955.1:n.1114C>T
ENST00000559931.5:c.286C>T	ENSP00000453446.1:n.286C>T
NM_005585.4:c.982C>T	NP_005576.3:p.Pro328Ser
NR_027654.1:n.2037C>T
XM_011521561.1:c.199C>T	XP_011519863.1:p.Pro67Ser
XR_931825.1:n.2381C>T
XM_011521561.2:c.199C>T	XP_011519863.1:p.Pro67Ser
NM_005585.5:c.982C>T MANE Select	NP_005576.3:p.Pro328Ser
NR_027654.2:n.2137C>T