Canonical Allele Identifier: CA2579539642
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640951G>T , CM000685.2:g.640951G>T GRCh38
NC_000023.10:g.601686G>T , CM000685.1:g.601686G>T GRCh37
NC_000023.9:g.521686G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.545-48G>T MANE Select ENSP00000508521.1:n.545-48G>T
ENST00000334060.8:c.545-48G>T ENSP00000335505.3:n.545-48G>T
ENST00000381575.6:c.545-48G>T ENSP00000370987.1:n.545-48G>T
ENST00000381578.6:c.545-48G>T ENSP00000370990.1:n.545-48G>T
ENST00000554971.6:c.545-48G>T ENSP00000452016.1:n.545-48G>T