Canonical Allele Identifier: CA169426575

Gene: SHH

Linked Data

• dbSNP Id: rs553827159
• gnomAD v2: 7-155605007-G-A
• gnomAD v3: 7-155812313-G-A
• gnomAD v4: 7-155812313-G-A
• MyVariant Identifiers: chr7:g.155605007G>A (hg19) ; chr7:g.155812313G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155812313G>A , CM000669.2:g.155812313G>A	GRCh38
NC_000007.13:g.155605007G>A , CM000669.1:g.155605007G>A	GRCh37
NC_000007.12:g.155297768G>A	NCBI36
NG_007504.2:g.4961C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297261.7:c.-191C>T MANE Select	ENSP00000297261.2:n.-191C>T
NM_000193.4:c.-191C>T MANE Select	NP_000184.1:n.-191C>T