Canonical Allele Identifier: CA783973290
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1167417948
gnomAD v3: 19-18787814-TC-T
gnomAD v4: 19-18787814-TC-T
MyVariant Identifiers: chr19:g.18898624del (hg19) chr19:g.18787815del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787817del , CM000681.2:g.18787817del GRCh38
NC_000019.9:g.18898626del , CM000681.1:g.18898626del GRCh37
NC_000019.8:g.18759626del NCBI36
NG_007070.1:g.8491del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-165del MANE Select ENSP00000222271.2:n.976-165del
ENST00000222271.6:c.976-165del ENSP00000222271.2:n.976-165del
ENST00000425807.1:c.817-165del ENSP00000403792.1:n.817-165del
ENST00000542601.6:c.877-165del ENSP00000439156.2:n.877-165del
NM_000095.2:c.976-165del NP_000086.2:n.976-165del
NM_000095.3:c.976-165del MANE Select NP_000086.2:n.976-165del
Search 100 bp 5'
Search 100 bp 3'