Canonical Allele Identifier: CA393201571

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781009-C-T
• MyVariant Identifiers: chr15:g.67073347C>T (hg19) ; chr15:g.66781009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781009C>T , CM000677.2:g.66781009C>T	GRCh38
NC_000015.9:g.67073347C>T , CM000677.1:g.67073347C>T	GRCh37
NC_000015.8:g.64860401C>T	NCBI36
NG_012244.1:g.83674C>T
NG_012244.2:g.83674C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.965C>T MANE Select	ENSP00000288840.5:p.Ser322Phe
ENST00000288840.9:c.965C>T	ENSP00000288840.5:p.Ser322Phe
ENST00000557916.5:c.1097C>T	ENSP00000452955.1:n.1097C>T
ENST00000559931.5:c.269C>T	ENSP00000453446.1:n.269C>T
NM_005585.4:c.965C>T	NP_005576.3:p.Ser322Phe
NR_027654.1:n.2020C>T
XM_011521561.1:c.182C>T	XP_011519863.1:p.Ser61Phe
XR_931825.1:n.2364C>T
XM_011521561.2:c.182C>T	XP_011519863.1:p.Ser61Phe
NM_005585.5:c.965C>T MANE Select	NP_005576.3:p.Ser322Phe
NR_027654.2:n.2120C>T