Canonical Allele Identifier: CA2326526625
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1601056714
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787984A>C , CM000681.2:g.18787984A>C GRCh38
NC_000019.9:g.18898793A>C , CM000681.1:g.18898793A>C GRCh37
NC_000019.8:g.18759793A>C NCBI36
NG_007070.1:g.8322T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.975+228T>G MANE Select ENSP00000222271.2:n.975+228T>G
ENST00000222271.6:c.975+228T>G ENSP00000222271.2:n.975+228T>G
ENST00000425807.1:c.816+228T>G ENSP00000403792.1:n.816+228T>G
ENST00000542601.6:c.876+228T>G ENSP00000439156.2:n.876+228T>G
NM_000095.2:c.975+228T>G NP_000086.2:n.975+228T>G
NM_000095.3:c.975+228T>G MANE Select NP_000086.2:n.975+228T>G
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