Canonical Allele Identifier: CA1109097375
Gene: SHH HGNC NCBI

Linked Data

dbSNP Id: rs1803541483
gnomAD v3: 7-155812324-A-T
gnomAD v4: 7-155812324-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812324A>T , CM000669.2:g.155812324A>T GRCh38
NC_000007.13:g.155605018A>T , CM000669.1:g.155605018A>T GRCh37
NC_000007.12:g.155297779A>T NCBI36
NG_007504.2:g.4950T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-202T>A MANE Select ENSP00000297261.2:n.-202T>A
NM_000193.4:c.-202T>A MANE Select NP_000184.1:n.-202T>A
Search 100 bp 5'
Search 100 bp 3'