Canonical Allele Identifier: CA2411385622
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634560C= , CM000685.2:g.634560C= GRCh38
NC_000023.10:g.595295C= , CM000685.1:g.595295C= GRCh37
NC_000023.9:g.515295C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.278-58C= MANE Select ENSP00000508521.1:n.278-58C=
ENST00000334060.8:c.278-58C= ENSP00000335505.3:n.278-58C=
ENST00000381575.6:c.278-58C= ENSP00000370987.1:n.278-58C=
ENST00000381578.6:c.278-58C= ENSP00000370990.1:n.278-58C=
ENST00000554971.6:c.278-58C= ENSP00000452016.1:n.278-58C=