Canonical Allele Identifier: CA1130295077
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs2052842541
gnomAD v3: X-640966-C-T
gnomAD v4: X-640966-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640966C>T , CM000685.2:g.640966C>T GRCh38
NC_000023.10:g.601701C>T , CM000685.1:g.601701C>T GRCh37
NC_000023.9:g.521701C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.545-33C>T MANE Select ENSP00000508521.1:n.545-33C>T
ENST00000334060.8:c.545-33C>T ENSP00000335505.3:n.545-33C>T
ENST00000381575.6:c.545-33C>T ENSP00000370987.1:n.545-33C>T
ENST00000381578.6:c.545-33C>T ENSP00000370990.1:n.545-33C>T
ENST00000554971.6:c.545-33C>T ENSP00000452016.1:n.545-33C>T