Canonical Allele Identifier: CA1754785076
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812374T= , CM000669.2:g.155812374T= GRCh38
NC_000007.13:g.155605068T= , CM000669.1:g.155605068T= GRCh37
NC_000007.12:g.155297829T= NCBI36
NG_007504.2:g.4900A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-252A= MANE Select ENSP00000297261.2:n.-252A=
NM_000193.4:c.-252A= MANE Select NP_000184.1:n.-252A=