Canonical Allele Identifier: CA2583623253
Gene: COMP HGNC NCBI

Linked Data

gnomAD v4: 19-18789314-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789314C>A , CM000681.2:g.18789314C>A GRCh38
NC_000019.9:g.18900123C>A , CM000681.1:g.18900123C>A GRCh37
NC_000019.8:g.18761123C>A NCBI36
NG_007070.1:g.6992G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.391-17G>T MANE Select ENSP00000222271.2:n.391-17G>T
ENST00000222271.6:c.391-17G>T ENSP00000222271.2:n.391-17G>T
ENST00000425807.1:c.391-422G>T ENSP00000403792.1:n.391-422G>T
ENST00000542601.6:c.292-17G>T ENSP00000439156.2:n.292-17G>T
NM_000095.2:c.391-17G>T NP_000086.2:n.391-17G>T
NM_000095.3:c.391-17G>T MANE Select NP_000086.2:n.391-17G>T
Search 100 bp 5'
Search 100 bp 3'