Canonical Allele Identifier: CA2184231508
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1894426134

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66774170A>T , CM000677.2:g.66774170A>T GRCh38
NC_000015.9:g.67066508A>T , CM000677.1:g.67066508A>T GRCh37
NC_000015.8:g.64853562A>T NCBI36
NG_012244.1:g.76835A>T
NG_012244.2:g.76835A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288840.10:c.953-6827A>T MANE Select ENSP00000288840.5:n.953-6827A>T
ENST00000288840.9:c.953-6827A>T ENSP00000288840.5:n.953-6827A>T
ENST00000557916.5:c.1085-6827A>T ENSP00000452955.1:n.1085-6827A>T
ENST00000559931.5:c.257-6827A>T ENSP00000453446.1:n.257-6827A>T
NM_005585.4:c.953-6827A>T NP_005576.3:n.953-6827A>T
NR_027654.1:n.2008-6827A>T
XM_011521561.1:c.170-6827A>T XP_011519863.1:n.170-6827A>T
XR_931825.1:n.2352-6827A>T
XM_011521561.2:c.170-6827A>T XP_011519863.1:n.170-6827A>T
NM_005585.5:c.953-6827A>T MANE Select NP_005576.3:n.953-6827A>T
NR_027654.2:n.2108-6827A>T