Canonical Allele Identifier: CA1742701597
Gene: SMO HGNC NCBI

Linked Data

dbSNP Id: rs1793910274

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129213299A>G , CM000669.2:g.129213299A>G GRCh38
NC_000007.13:g.128853140A>G , CM000669.1:g.128853140A>G GRCh37
NC_000007.12:g.128640376A>G NCBI36
NG_023340.1:g.29428A>G
NG_023340.2:g.29428A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249373.8:c.*848A>G MANE Select ENSP00000249373.3:n.*848A>G
ENST00000655644.1:c.*2967A>G ENSP00000499377.1:n.*2967A>G
ENST00000249373.7:c.*848A>G ENSP00000249373.3:n.*848A>G
NM_005631.4:c.*848A>G NP_005622.1:n.*848A>G
XM_011516522.1:c.*848A>G XP_011514824.1:n.*848A>G
XM_024446891.1:c.*848A>G XP_024302659.1:n.*848A>G
NM_005631.5:c.*848A>G MANE Select NP_005622.1:n.*848A>G