Canonical Allele Identifier: CA783973315
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1555791604
gnomAD v2: 19-18898655-T-TTC
gnomAD v3: 19-18787846-T-TTC
gnomAD v4: 19-18787846-T-TTC
MyVariant Identifiers: chr19:g.18898655_18898656insTC (hg19) chr19:g.18787846_18787847insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787847_18787848insCT , CM000681.2:g.18787847_18787848insCT GRCh38
NC_000019.9:g.18898656_18898657insCT , CM000681.1:g.18898656_18898657insCT GRCh37
NC_000019.8:g.18759656_18759657insCT NCBI36
NG_007070.1:g.8459_8460insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-197_976-196insGA MANE Select ENSP00000222271.2:n.976-197_976-196insGA
ENST00000222271.6:c.976-197_976-196insGA ENSP00000222271.2:n.976-197_976-196insGA
ENST00000425807.1:c.817-197_817-196insGA ENSP00000403792.1:n.817-197_817-196insGA
ENST00000542601.6:c.877-197_877-196insGA ENSP00000439156.2:n.877-197_877-196insGA
NM_000095.2:c.976-197_976-196insGA NP_000086.2:n.976-197_976-196insGA
NM_000095.3:c.976-197_976-196insGA MANE Select NP_000086.2:n.976-197_976-196insGA
Search 100 bp 5'
Search 100 bp 3'