Canonical Allele Identifier: CA1742701578
Gene: SMO HGNC NCBI

Linked Data

dbSNP Id: rs1584667587

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129213286C>T , CM000669.2:g.129213286C>T GRCh38
NC_000007.13:g.128853127C>T , CM000669.1:g.128853127C>T GRCh37
NC_000007.12:g.128640363C>T NCBI36
NG_023340.1:g.29415C>T
NG_023340.2:g.29415C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249373.8:c.*835C>T MANE Select ENSP00000249373.3:n.*835C>T
ENST00000655644.1:c.*2954C>T ENSP00000499377.1:n.*2954C>T
ENST00000249373.7:c.*835C>T ENSP00000249373.3:n.*835C>T
NM_005631.4:c.*835C>T NP_005622.1:n.*835C>T
XM_011516522.1:c.*835C>T XP_011514824.1:n.*835C>T
XM_024446891.1:c.*835C>T XP_024302659.1:n.*835C>T
NM_005631.5:c.*835C>T MANE Select NP_005622.1:n.*835C>T