Canonical Allele Identifier: CA1754784889
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812287A= , CM000669.2:g.155812287A= GRCh38
NC_000007.13:g.155604981A= , CM000669.1:g.155604981A= GRCh37
NC_000007.12:g.155297742A= NCBI36
NG_007504.2:g.4987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-165T= MANE Select ENSP00000297261.2:n.-165T=
NM_000193.4:c.-165T= MANE Select NP_000184.1:n.-165T=