Canonical Allele Identifier: CA213114
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.624528G>C , CM000685.2:g.624528G>C GRCh38
NC_000023.10:g.585263G>C , CM000685.1:g.585263G>C GRCh37
NC_000023.9:g.505263G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334060.8:c.-507G>C ENSP00000335505.3:n.-507G>C
ENST00000381578.6:c.-507G>C ENSP00000370990.1:n.-507G>C