Canonical Allele Identifier: CA393201682

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781059-C-T
• MyVariant Identifiers: chr15:g.67073397C>T (hg19) ; chr15:g.66781059C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781059C>T , CM000677.2:g.66781059C>T	GRCh38
NC_000015.9:g.67073397C>T , CM000677.1:g.67073397C>T	GRCh37
NC_000015.8:g.64860451C>T	NCBI36
NG_012244.1:g.83724C>T
NG_012244.2:g.83724C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1015C>T MANE Select	ENSP00000288840.5:p.His339Tyr
ENST00000288840.9:c.1015C>T	ENSP00000288840.5:p.His339Tyr
ENST00000557916.5:c.1147C>T	ENSP00000452955.1:n.1147C>T
ENST00000559931.5:c.319C>T	ENSP00000453446.1:n.319C>T
NM_005585.4:c.1015C>T	NP_005576.3:p.His339Tyr
NR_027654.1:n.2070C>T
XM_011521561.1:c.232C>T	XP_011519863.1:p.His78Tyr
XR_931825.1:n.2414C>T
XM_011521561.2:c.232C>T	XP_011519863.1:p.His78Tyr
NM_005585.5:c.1015C>T MANE Select	NP_005576.3:p.His339Tyr
NR_027654.2:n.2170C>T