Canonical Allele Identifier: CA1754784882
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812273C= , CM000669.2:g.155812273C= GRCh38
NC_000007.13:g.155604967C= , CM000669.1:g.155604967C= GRCh37
NC_000007.12:g.155297728C= NCBI36
NG_007504.2:g.5001G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-151G= MANE Select ENSP00000297261.2:n.-151G=
ENST00000297261.6:c.-151G= ENSP00000297261.2:n.-151G=
NM_000193.2:c.-151G= NP_000184.1:n.-151G=
NM_000193.3:c.-151G= NP_000184.1:n.-151G=
NM_000193.4:c.-151G= MANE Select NP_000184.1:n.-151G=