Canonical Allele Identifier: CA169426606

Gene: SHH

Linked Data

• dbSNP Id: rs749947576
• gnomAD v2: 7-155605081-C-T
• gnomAD v3: 7-155812387-C-T
• gnomAD v4: 7-155812387-C-T
• MyVariant Identifiers: chr7:g.155605081C>T (hg19) ; chr7:g.155812387C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155812387C>T , CM000669.2:g.155812387C>T	GRCh38
NC_000007.13:g.155605081C>T , CM000669.1:g.155605081C>T	GRCh37
NC_000007.12:g.155297842C>T	NCBI36
NG_007504.2:g.4887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297261.7:c.-265G>A MANE Select	ENSP00000297261.2:n.-265G>A
NM_000193.4:c.-265G>A MANE Select	NP_000184.1:n.-265G>A