Canonical Allele Identifier: CA515393308
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs2052712822
MyVariant Identifiers: chrX:g.595477A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634742A>G , CM000685.2:g.634742A>G GRCh38
NC_000023.10:g.595477A>G , CM000685.1:g.595477A>G GRCh37
NC_000023.9:g.515477A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.402A>G MANE Select ENSP00000508521.1:p.Arg134=
ENST00000334060.8:c.402A>G ENSP00000335505.3:p.Arg134=
ENST00000381575.6:c.402A>G ENSP00000370987.1:p.Arg134=
ENST00000381578.6:c.402A>G ENSP00000370990.1:p.Arg134=
ENST00000554971.6:c.402A>G ENSP00000452016.1:p.Arg134=
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