Canonical Allele Identifier: CA1754784760
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812215C= , CM000669.2:g.155812215C= GRCh38
NC_000007.13:g.155604909C= , CM000669.1:g.155604909C= GRCh37
NC_000007.12:g.155297670C= NCBI36
NG_007504.2:g.5059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-93G= MANE Select ENSP00000297261.2:n.-93G=
ENST00000297261.6:c.-93G= ENSP00000297261.2:n.-93G=
NM_000193.2:c.-93G= NP_000184.1:n.-93G=
NM_000193.3:c.-93G= NP_000184.1:n.-93G=
NM_000193.4:c.-93G= MANE Select NP_000184.1:n.-93G=