Canonical Allele Identifier: CA412231626
Gene: SHOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640828T>C , CM000685.2:g.640828T>C GRCh38
NC_000023.10:g.601563T>C , CM000685.1:g.601563T>C GRCh37
NC_000023.9:g.521563T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.494T>C MANE Select ENSP00000508521.1:p.Phe165Ser
ENST00000334060.8:c.494T>C ENSP00000335505.3:p.Phe165Ser
ENST00000381575.6:c.494T>C ENSP00000370987.1:p.Phe165Ser
ENST00000381578.6:c.494T>C ENSP00000370990.1:p.Phe165Ser
ENST00000554971.6:c.494T>C ENSP00000452016.1:p.Phe165Ser