Canonical Allele Identifier: CA1754784714

Gene: SHH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155812191T= , CM000669.2:g.155812191T=	GRCh38
NC_000007.13:g.155604885T= , CM000669.1:g.155604885T=	GRCh37
NC_000007.12:g.155297646T=	NCBI36
NG_007504.2:g.5083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297261.7:c.-69A= MANE Select	ENSP00000297261.2:n.-69A=
ENST00000297261.6:c.-69A=	ENSP00000297261.2:n.-69A=
NM_000193.2:c.-69A=	NP_000184.1:n.-69A=
NM_000193.3:c.-69A=	NP_000184.1:n.-69A=
NM_000193.4:c.-69A= MANE Select	NP_000184.1:n.-69A=