Canonical Allele Identifier: CA2326526337
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs2055178316
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787811A>G , CM000681.2:g.18787811A>G GRCh38
NC_000019.9:g.18898620A>G , CM000681.1:g.18898620A>G GRCh37
NC_000019.8:g.18759620A>G NCBI36
NG_007070.1:g.8495T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-161T>C MANE Select ENSP00000222271.2:n.976-161T>C
ENST00000222271.6:c.976-161T>C ENSP00000222271.2:n.976-161T>C
ENST00000425807.1:c.817-161T>C ENSP00000403792.1:n.817-161T>C
ENST00000542601.6:c.877-161T>C ENSP00000439156.2:n.877-161T>C
NM_000095.2:c.976-161T>C NP_000086.2:n.976-161T>C
NM_000095.3:c.976-161T>C MANE Select NP_000086.2:n.976-161T>C
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