Canonical Allele Identifier: CA306257015
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1555791613
MyVariant Identifiers: chr19:g.18898678_18898679del (hg19) chr19:g.18787869_18787870del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787870_18787871del , CM000681.2:g.18787870_18787871del GRCh38
NC_000019.9:g.18898679_18898680del , CM000681.1:g.18898679_18898680del GRCh37
NC_000019.8:g.18759679_18759680del NCBI36
NG_007070.1:g.8436_8437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-220_976-219del MANE Select ENSP00000222271.2:n.976-220_976-219del
ENST00000222271.6:c.976-220_976-219del ENSP00000222271.2:n.976-220_976-219del
ENST00000425807.1:c.817-220_817-219del ENSP00000403792.1:n.817-220_817-219del
ENST00000542601.6:c.877-220_877-219del ENSP00000439156.2:n.877-220_877-219del
NM_000095.2:c.976-220_976-219del NP_000086.2:n.976-220_976-219del
NM_000095.3:c.976-220_976-219del MANE Select NP_000086.2:n.976-220_976-219del
Search 100 bp 5'
Search 100 bp 3'