Canonical Allele Identifier: CA272023028

Gene: SMAD6

Linked Data

• dbSNP Id: rs1041376711
• gnomAD v3: 15-66780861-G-A
• gnomAD v4: 15-66780861-G-A
• MyVariant Identifiers: chr15:g.67073199G>A (hg19) ; chr15:g.66780861G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66780861G>A , CM000677.2:g.66780861G>A	GRCh38
NC_000015.9:g.67073199G>A , CM000677.1:g.67073199G>A	GRCh37
NC_000015.8:g.64860253G>A	NCBI36
NG_012244.1:g.83526G>A
NG_012244.2:g.83526G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.953-136G>A MANE Select	ENSP00000288840.5:n.953-136G>A
ENST00000288840.9:c.953-136G>A	ENSP00000288840.5:n.953-136G>A
ENST00000557916.5:c.1085-136G>A	ENSP00000452955.1:n.1085-136G>A
ENST00000559931.5:c.257-136G>A	ENSP00000453446.1:n.257-136G>A
NM_005585.4:c.953-136G>A	NP_005576.3:n.953-136G>A
NR_027654.1:n.2008-136G>A
XM_011521561.1:c.170-136G>A	XP_011519863.1:n.170-136G>A
XR_931825.1:n.2352-136G>A
XM_011521561.2:c.170-136G>A	XP_011519863.1:n.170-136G>A
NM_005585.5:c.953-136G>A MANE Select	NP_005576.3:n.953-136G>A
NR_027654.2:n.2108-136G>A