Canonical Allele Identifier: CA515393199
Gene: SHOX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.595444C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634709C>T , CM000685.2:g.634709C>T GRCh38
NC_000023.10:g.595444C>T , CM000685.1:g.595444C>T GRCh37
NC_000023.9:g.515444C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.369C>T MANE Select ENSP00000508521.1:p.Asn123=
ENST00000334060.8:c.369C>T ENSP00000335505.3:p.Asn123=
ENST00000381575.6:c.369C>T ENSP00000370987.1:p.Asn123=
ENST00000381578.6:c.369C>T ENSP00000370990.1:p.Asn123=
ENST00000554971.6:c.369C>T ENSP00000452016.1:p.Asn123=
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