Canonical Allele Identifier: CA2692951859
Gene: SHOX HGNC NCBI

Linked Data

gnomAD v4: X-634559-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634559T>C , CM000685.2:g.634559T>C GRCh38
NC_000023.10:g.595294T>C , CM000685.1:g.595294T>C GRCh37
NC_000023.9:g.515294T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.278-59T>C MANE Select ENSP00000508521.1:n.278-59T>C
ENST00000334060.8:c.278-59T>C ENSP00000335505.3:n.278-59T>C
ENST00000381575.6:c.278-59T>C ENSP00000370987.1:n.278-59T>C
ENST00000381578.6:c.278-59T>C ENSP00000370990.1:n.278-59T>C
ENST00000554971.6:c.278-59T>C ENSP00000452016.1:n.278-59T>C