Canonical Allele Identifier: CA515393277
Gene: SHOX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.595471C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634736C>T , CM000685.2:g.634736C>T GRCh38
NC_000023.10:g.595471C>T , CM000685.1:g.595471C>T GRCh37
NC_000023.9:g.515471C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.396C>T MANE Select ENSP00000508521.1:p.Leu132=
ENST00000334060.8:c.396C>T ENSP00000335505.3:p.Leu132=
ENST00000381575.6:c.396C>T ENSP00000370987.1:p.Leu132=
ENST00000381578.6:c.396C>T ENSP00000370990.1:p.Leu132=
ENST00000554971.6:c.396C>T ENSP00000452016.1:p.Leu132=