Canonical Allele Identifier: CA1754783972

Gene: SHH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155812038C= , CM000669.2:g.155812038C=	GRCh38
NC_000007.13:g.155604732C= , CM000669.1:g.155604732C=	GRCh37
NC_000007.12:g.155297493C=	NCBI36
NG_007504.2:g.5236G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297261.7:c.85G= MANE Select	ENSP00000297261.2:p.Gly29=
ENST00000297261.6:c.85G=	ENSP00000297261.2:p.Gly29=
NM_000193.2:c.85G=	NP_000184.1:p.Gly29=
NM_000193.3:c.85G=	NP_000184.1:p.Gly29=
NM_000193.4:c.85G= MANE Select	NP_000184.1:p.Gly29=