Canonical Allele Identifier: CA169426562
Gene: SHH HGNC NCBI

Linked Data

dbSNP Id: rs945500832
gnomAD v3: 7-155812303-C-A
gnomAD v4: 7-155812303-C-A
MyVariant Identifiers: chr7:g.155604997C>A (hg19) chr7:g.155812303C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812303C>A , CM000669.2:g.155812303C>A GRCh38
NC_000007.13:g.155604997C>A , CM000669.1:g.155604997C>A GRCh37
NC_000007.12:g.155297758C>A NCBI36
NG_007504.2:g.4971G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-181G>T MANE Select ENSP00000297261.2:n.-181G>T
NM_000193.4:c.-181G>T MANE Select NP_000184.1:n.-181G>T
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Search 100 bp 3'