Canonical Allele Identifier: CA10330039
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs749938493
ExAC: X:601634 G / T
gnomAD v2: X-601634-G-T
gnomAD v3: X-640899-G-T
gnomAD v4: X-640899-G-T
MyVariant Identifiers: chrX:g.601634G>T (hg19) chrX:g.640899G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640899G>T , CM000685.2:g.640899G>T GRCh38
NC_000023.10:g.601634G>T , CM000685.1:g.601634G>T GRCh37
NC_000023.9:g.521634G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.544+21G>T MANE Select ENSP00000508521.1:n.544+21G>T
ENST00000334060.8:c.544+21G>T ENSP00000335505.3:n.544+21G>T
ENST00000381575.6:c.544+21G>T ENSP00000370987.1:n.544+21G>T
ENST00000381578.6:c.544+21G>T ENSP00000370990.1:n.544+21G>T
ENST00000554971.6:c.544+21G>T ENSP00000452016.1:n.544+21G>T
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