Canonical Allele Identifier: CA14134564
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs2053423

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66733879C>T , CM000677.2:g.66733879C>T GRCh38
NC_000015.9:g.67026217C>T , CM000677.1:g.67026217C>T GRCh37
NC_000015.8:g.64813271C>T NCBI36
NG_012244.1:g.36544C>T
NG_012244.2:g.36544C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.952+17381C>T MANE Select ENSP00000288840.5:n.952+17381C>T
ENST00000288840.9:c.952+17381C>T ENSP00000288840.5:n.952+17381C>T
ENST00000557916.5:c.1084+16739C>T ENSP00000452955.1:n.1084+16739C>T
ENST00000559931.5:c.256+16739C>T ENSP00000453446.1:n.256+16739C>T
NM_005585.4:c.952+17381C>T NP_005576.3:n.952+17381C>T
NR_027654.1:n.2007+16739C>T
XM_011521561.1:c.169+17381C>T XP_011519863.1:n.169+17381C>T
XR_931825.1:n.2351+17381C>T
XM_011521561.2:c.169+17381C>T XP_011519863.1:n.169+17381C>T
NM_005585.5:c.952+17381C>T MANE Select NP_005576.3:n.952+17381C>T
NR_027654.2:n.2107+16739C>T