Canonical Allele Identifier: CA1754784753
Gene: SHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812209C= , CM000669.2:g.155812209C= GRCh38
NC_000007.13:g.155604903C= , CM000669.1:g.155604903C= GRCh37
NC_000007.12:g.155297664C= NCBI36
NG_007504.2:g.5065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-87G= MANE Select ENSP00000297261.2:n.-87G=
ENST00000297261.6:c.-87G= ENSP00000297261.2:n.-87G=
NM_000193.2:c.-87G= NP_000184.1:n.-87G=
NM_000193.3:c.-87G= NP_000184.1:n.-87G=
NM_000193.4:c.-87G= MANE Select NP_000184.1:n.-87G=
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