Canonical Allele Identifier: CA1754784656

Gene: SHH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155812172C= , CM000669.2:g.155812172C=	GRCh38
NC_000007.13:g.155604866C= , CM000669.1:g.155604866C=	GRCh37
NC_000007.12:g.155297627C=	NCBI36
NG_007504.2:g.5102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297261.7:c.-50G= MANE Select	ENSP00000297261.2:n.-50G=
ENST00000297261.6:c.-50G=	ENSP00000297261.2:n.-50G=
NM_000193.2:c.-50G=	NP_000184.1:n.-50G=
NM_000193.3:c.-50G=	NP_000184.1:n.-50G=
NM_000193.4:c.-50G= MANE Select	NP_000184.1:n.-50G=