Canonical Allele Identifier: CA506053137
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1555791611
gnomAD v3: 19-18787864-CTCTT-C
gnomAD v4: 19-18787864-CTCTT-C
MyVariant Identifiers: chr19:g.18898674_18898677del (hg19) chr19:g.18787865_18787868del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787914_18787917del , CM000681.2:g.18787914_18787917del GRCh38
NC_000019.9:g.18898723_18898726del , CM000681.1:g.18898723_18898726del GRCh37
NC_000019.8:g.18759723_18759726del NCBI36
NG_007070.1:g.8438_8441del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-218_976-215del MANE Select ENSP00000222271.2:n.976-218_976-215del
ENST00000222271.6:c.976-218_976-215del ENSP00000222271.2:n.976-218_976-215del
ENST00000425807.1:c.817-218_817-215del ENSP00000403792.1:n.817-218_817-215del
ENST00000542601.6:c.877-218_877-215del ENSP00000439156.2:n.877-218_877-215del
NM_000095.2:c.976-218_976-215del NP_000086.2:n.976-218_976-215del
NM_000095.3:c.976-218_976-215del MANE Select NP_000086.2:n.976-218_976-215del
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