Canonical Allele Identifier: CA393201804
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs374240137

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781118C>A , CM000677.2:g.66781118C>A GRCh38
NC_000015.9:g.67073456C>A , CM000677.1:g.67073456C>A GRCh37
NC_000015.8:g.64860510C>A NCBI36
NG_012244.1:g.83783C>A
NG_012244.2:g.83783C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1074C>A MANE Select ENSP00000288840.5:p.Tyr358Ter
ENST00000288840.9:c.1074C>A ENSP00000288840.5:p.Tyr358Ter
ENST00000557916.5:c.1206C>A ENSP00000452955.1:n.1206C>A
ENST00000559931.5:c.378C>A ENSP00000453446.1:n.378C>A
NM_005585.4:c.1074C>A NP_005576.3:p.Tyr358Ter
NR_027654.1:n.2129C>A
XM_011521561.1:c.291C>A XP_011519863.1:p.Tyr97Ter
XR_931825.1:n.2473C>A
XM_011521561.2:c.291C>A XP_011519863.1:p.Tyr97Ter
NM_005585.5:c.1074C>A MANE Select NP_005576.3:p.Tyr358Ter
NR_027654.2:n.2229C>A