Canonical Allele Identifier: CA1754784782
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812230G= , CM000669.2:g.155812230G= GRCh38
NC_000007.13:g.155604924G= , CM000669.1:g.155604924G= GRCh37
NC_000007.12:g.155297685G= NCBI36
NG_007504.2:g.5044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-108C= MANE Select ENSP00000297261.2:n.-108C=
ENST00000297261.6:c.-108C= ENSP00000297261.2:n.-108C=
NM_000193.2:c.-108C= NP_000184.1:n.-108C=
NM_000193.3:c.-108C= NP_000184.1:n.-108C=
NM_000193.4:c.-108C= MANE Select NP_000184.1:n.-108C=