Canonical Allele Identifier: CA1754785079
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812375A= , CM000669.2:g.155812375A= GRCh38
NC_000007.13:g.155605069A= , CM000669.1:g.155605069A= GRCh37
NC_000007.12:g.155297830A= NCBI36
NG_007504.2:g.4899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-253T= MANE Select ENSP00000297261.2:n.-253T=
NM_000193.4:c.-253T= MANE Select NP_000184.1:n.-253T=