Canonical Allele Identifier: CA306256900
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs754581392
MyVariant Identifiers: chr19:g.18898644_18898647del (hg19) chr19:g.18787835_18787838del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787838_18787841del , CM000681.2:g.18787838_18787841del GRCh38
NC_000019.9:g.18898647_18898650del , CM000681.1:g.18898647_18898650del GRCh37
NC_000019.8:g.18759647_18759650del NCBI36
NG_007070.1:g.8468_8471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-188_976-185del MANE Select ENSP00000222271.2:n.976-188_976-185del
ENST00000222271.6:c.976-188_976-185del ENSP00000222271.2:n.976-188_976-185del
ENST00000425807.1:c.817-188_817-185del ENSP00000403792.1:n.817-188_817-185del
ENST00000542601.6:c.877-188_877-185del ENSP00000439156.2:n.877-188_877-185del
NM_000095.2:c.976-188_976-185del NP_000086.2:n.976-188_976-185del
NM_000095.3:c.976-188_976-185del MANE Select NP_000086.2:n.976-188_976-185del
Search 100 bp 5'
Search 100 bp 3'