Canonical Allele Identifier: CA2411389737
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs2052840239

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640816C>G , CM000685.2:g.640816C>G GRCh38
NC_000023.10:g.601551C>G , CM000685.1:g.601551C>G GRCh37
NC_000023.9:g.521551C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.487-5C>G MANE Select ENSP00000508521.1:n.487-5C>G
ENST00000334060.8:c.487-5C>G ENSP00000335505.3:n.487-5C>G
ENST00000381575.6:c.487-5C>G ENSP00000370987.1:n.487-5C>G
ENST00000381578.6:c.487-5C>G ENSP00000370990.1:n.487-5C>G
ENST00000554971.6:c.487-5C>G ENSP00000452016.1:n.487-5C>G