Canonical Allele Identifier: CA876809659
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.624389_624390insGTG , CM000685.2:g.624389_624390insGTG GRCh38
NC_000023.10:g.585124_585125insGTG , CM000685.1:g.585124_585125insGTG GRCh37
NC_000023.9:g.505124_505125insGTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334060.8:c.-646_-645insGTG ENSP00000335505.3:n.-646_-645insGTG
ENST00000381578.6:c.-646_-645insGTG ENSP00000370990.1:n.-646_-645insGTG