Canonical Allele Identifier: CA1742695586
Gene: SMO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129210502G= , CM000669.2:g.129210502G= GRCh38
NC_000007.13:g.128850343G= , CM000669.1:g.128850343G= GRCh37
NC_000007.12:g.128637579G= NCBI36
NG_023340.1:g.26631G=
NG_023340.2:g.26631G=

Transcript Alleles

HGVS Amino-acid change
ENST00000249373.8:c.1606G= MANE Select ENSP00000249373.3:p.Val536=
ENST00000655644.1:c.*1361G= ENSP00000499377.1:n.*1361G=
ENST00000249373.7:c.1606G= ENSP00000249373.3:p.Val536=
ENST00000462420.2:c.577G=
NM_005631.4:c.1606G= NP_005622.1:p.Val536=
XM_011516522.1:c.1216G= XP_011514824.1:p.Val406=
XM_024446891.1:c.1216G= XP_024302659.1:p.Val406=
NM_005631.5:c.1606G= MANE Select NP_005622.1:p.Val536=