Canonical Allele Identifier: CA458893501
Gene: SHH HGNC NCBI

Linked Data

COSMIC: COSM3636701
MyVariant Identifiers: chr7:g.155604733C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812039C>T , CM000669.2:g.155812039C>T GRCh38
NC_000007.13:g.155604733C>T , CM000669.1:g.155604733C>T GRCh37
NC_000007.12:g.155297494C>T NCBI36
NG_007504.2:g.5235G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297261.7:c.84G>A MANE Select ENSP00000297261.2:p.Arg28=
ENST00000297261.6:c.84G>A ENSP00000297261.2:p.Arg28=
NM_000193.2:c.84G>A NP_000184.1:p.Arg28=
NM_000193.3:c.84G>A NP_000184.1:p.Arg28=
NM_000193.4:c.84G>A MANE Select NP_000184.1:p.Arg28=
Search 100 bp 5'
Search 100 bp 3'