Canonical Allele Identifier: CA1742701642
Gene: SMO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129213302T= , CM000669.2:g.129213302T= GRCh38
NC_000007.13:g.128853143T= , CM000669.1:g.128853143T= GRCh37
NC_000007.12:g.128640379T= NCBI36
NG_023340.1:g.29431T=
NG_023340.2:g.29431T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249373.8:c.*851T= MANE Select ENSP00000249373.3:n.*851T=
ENST00000655644.1:c.*2970T= ENSP00000499377.1:n.*2970T=
ENST00000249373.7:c.*851T= ENSP00000249373.3:n.*851T=
NM_005631.4:c.*851T= NP_005622.1:n.*851T=
XM_011516522.1:c.*851T= XP_011514824.1:n.*851T=
XM_024446891.1:c.*851T= XP_024302659.1:n.*851T=
NM_005631.5:c.*851T= MANE Select NP_005622.1:n.*851T=
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