Canonical Allele Identifier: CA1754783979
Gene: SHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812039C= , CM000669.2:g.155812039C= GRCh38
NC_000007.13:g.155604733C= , CM000669.1:g.155604733C= GRCh37
NC_000007.12:g.155297494C= NCBI36
NG_007504.2:g.5235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297261.7:c.84G= MANE Select ENSP00000297261.2:p.Arg28=
ENST00000297261.6:c.84G= ENSP00000297261.2:p.Arg28=
NM_000193.2:c.84G= NP_000184.1:p.Arg28=
NM_000193.3:c.84G= NP_000184.1:p.Arg28=
NM_000193.4:c.84G= MANE Select NP_000184.1:p.Arg28=