Canonical Allele Identifier: CA640120837
Gene: SHOX HGNC NCBI

Linked Data

dbSNP Id: rs1247968285
gnomAD v2: X-601483-G-A
gnomAD v3: X-640748-G-A
gnomAD v4: X-640748-G-A
MyVariant Identifiers: chrX:g.601483G>A (hg19) chrX:g.640748G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.640748G>A , CM000685.2:g.640748G>A GRCh38
NC_000023.10:g.601483G>A , CM000685.1:g.601483G>A GRCh37
NC_000023.9:g.521483G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.487-73G>A MANE Select ENSP00000508521.1:n.487-73G>A
ENST00000334060.8:c.487-73G>A ENSP00000335505.3:n.487-73G>A
ENST00000381575.6:c.487-73G>A ENSP00000370987.1:n.487-73G>A
ENST00000381578.6:c.487-73G>A ENSP00000370990.1:n.487-73G>A
ENST00000554971.6:c.487-73G>A ENSP00000452016.1:n.487-73G>A
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