Canonical Allele Identifier: CA2326525621
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1601054118
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786193T>G , CM000681.2:g.18786193T>G GRCh38
NC_000019.9:g.18897003T>G , CM000681.1:g.18897003T>G GRCh37
NC_000019.8:g.18758003T>G NCBI36
NG_007070.1:g.10112A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-47A>C MANE Select ENSP00000222271.2:n.1308-47A>C
ENST00000222271.6:c.1308-47A>C ENSP00000222271.2:n.1308-47A>C
ENST00000425807.1:c.1149-47A>C ENSP00000403792.1:n.1149-47A>C
ENST00000542601.6:c.1209-47A>C ENSP00000439156.2:n.1209-47A>C
ENST00000612179.1:n.558-47A>C
NM_000095.2:c.1308-47A>C NP_000086.2:n.1308-47A>C
NM_000095.3:c.1308-47A>C MANE Select NP_000086.2:n.1308-47A>C
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