Canonical Allele Identifier: CA369247106
Gene: SMO HGNC NCBI

Linked Data

dbSNP Id: rs121918347

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129210500G>A , CM000669.2:g.129210500G>A GRCh38
NC_000007.13:g.128850341G>A , CM000669.1:g.128850341G>A GRCh37
NC_000007.12:g.128637577G>A NCBI36
NG_023340.1:g.26629G>A
NG_023340.2:g.26629G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000249373.8:c.1604G>A MANE Select ENSP00000249373.3:p.Trp535Ter
ENST00000655644.1:c.*1359G>A ENSP00000499377.1:n.*1359G>A
ENST00000249373.7:c.1604G>A ENSP00000249373.3:p.Trp535Ter
ENST00000462420.2:c.575G>A
NM_005631.4:c.1604G>A NP_005622.1:p.Trp535Ter
XM_011516522.1:c.1214G>A XP_011514824.1:p.Trp405Ter
XM_024446891.1:c.1214G>A XP_024302659.1:p.Trp405Ter
NM_005631.5:c.1604G>A MANE Select NP_005622.1:p.Trp535Ter