Canonical Allele Identifier: CA10330062
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs752536855
ExAC: X:601748 A / G
gnomAD v2: X-601748-A-G
gnomAD v4: X-641013-A-G
MyVariant Identifiers: chrX:g.601748A>G (hg19) chrX:g.641013A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.641013A>G , CM000685.2:g.641013A>G GRCh38
NC_000023.10:g.601748A>G , CM000685.1:g.601748A>G GRCh37
NC_000023.9:g.521748A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.559A>G MANE Select ENSP00000508521.1:p.Thr187Ala
ENST00000334060.8:c.559A>G ENSP00000335505.3:p.Thr187Ala
ENST00000381575.6:c.559A>G ENSP00000370987.1:p.Thr187Ala
ENST00000381578.6:c.559A>G ENSP00000370990.1:p.Thr187Ala
ENST00000554971.6:c.559A>G ENSP00000452016.1:p.Thr187Ala
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