Canonical Allele Identifier: CA370152097
Gene: SHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.155604692A>T (hg19) chr7:g.155811998A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155811998A>T , CM000669.2:g.155811998A>T GRCh38
NC_000007.13:g.155604692A>T , CM000669.1:g.155604692A>T GRCh37
NC_000007.12:g.155297453A>T NCBI36
NG_007504.2:g.5276T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.125T>A MANE Select ENSP00000297261.2:p.Leu42Ter
ENST00000297261.6:c.125T>A ENSP00000297261.2:p.Leu42Ter
NM_000193.2:c.125T>A NP_000184.1:p.Leu42Ter
NM_000193.3:c.125T>A NP_000184.1:p.Leu42Ter
NM_000193.4:c.125T>A MANE Select NP_000184.1:p.Leu42Ter
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