Canonical Allele Identifier: CA1754784988
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812329T= , CM000669.2:g.155812329T= GRCh38
NC_000007.13:g.155605023T= , CM000669.1:g.155605023T= GRCh37
NC_000007.12:g.155297784T= NCBI36
NG_007504.2:g.4945A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-207A= MANE Select ENSP00000297261.2:n.-207A=
NM_000193.4:c.-207A= MANE Select NP_000184.1:n.-207A=