Canonical Allele Identifier: CA2695231051
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634827del , CM000685.2:g.634827del GRCh38
NC_000023.10:g.595562del , CM000685.1:g.595562del GRCh37
NC_000023.9:g.515562del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.486+1del
ENST00000334060.8:c.486+1del
ENST00000381575.6:c.486+1del
ENST00000381578.6:c.486+1del
ENST00000554971.6:c.486+1del