Canonical Allele Identifier: CA2692951860
Gene: SHOX HGNC NCBI

Linked Data

gnomAD v4: X-634561-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634561G>T , CM000685.2:g.634561G>T GRCh38
NC_000023.10:g.595296G>T , CM000685.1:g.595296G>T GRCh37
NC_000023.9:g.515296G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.278-57G>T MANE Select ENSP00000508521.1:n.278-57G>T
ENST00000334060.8:c.278-57G>T ENSP00000335505.3:n.278-57G>T
ENST00000381575.6:c.278-57G>T ENSP00000370987.1:n.278-57G>T
ENST00000381578.6:c.278-57G>T ENSP00000370990.1:n.278-57G>T
ENST00000554971.6:c.278-57G>T ENSP00000452016.1:n.278-57G>T