Canonical Allele Identifier: CA214246
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs193922466
gnomAD v2: X-595422-A-G
gnomAD v3: X-634687-A-G
gnomAD v4: X-634687-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634687A>G , CM000685.2:g.634687A>G GRCh38
NC_000023.10:g.595422A>G , CM000685.1:g.595422A>G GRCh37
NC_000023.9:g.515422A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.347A>G MANE Select ENSP00000508521.1:p.Lys116Arg
ENST00000334060.8:c.347A>G ENSP00000335505.3:p.Lys116Arg
ENST00000381575.6:c.347A>G ENSP00000370987.1:p.Lys116Arg
ENST00000381578.6:c.347A>G ENSP00000370990.1:p.Lys116Arg
ENST00000554971.6:c.347A>G ENSP00000452016.1:p.Lys116Arg