Canonical Allele Identifier: CA306257030
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs201767586
MyVariant Identifiers: chr19:g.18898681_18898682insTC (hg19) chr19:g.18787872_18787873insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787874_18787875dup , CM000681.2:g.18787874_18787875dup GRCh38
NC_000019.9:g.18898683_18898684dup , CM000681.1:g.18898683_18898684dup GRCh37
NC_000019.8:g.18759683_18759684dup NCBI36
NG_007070.1:g.8432_8433dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-224_976-223dup MANE Select ENSP00000222271.2:n.976-224_976-223dup
ENST00000222271.6:c.976-224_976-223dup ENSP00000222271.2:n.976-224_976-223dup
ENST00000425807.1:c.817-224_817-223dup ENSP00000403792.1:n.817-224_817-223dup
ENST00000542601.6:c.877-224_877-223dup ENSP00000439156.2:n.877-224_877-223dup
NM_000095.2:c.976-224_976-223dup NP_000086.2:n.976-224_976-223dup
NM_000095.3:c.976-224_976-223dup MANE Select NP_000086.2:n.976-224_976-223dup
Search 100 bp 5'
Search 100 bp 3'