Canonical Allele Identifier: CA2583623241
Gene: COMP HGNC NCBI

Linked Data

gnomAD v4: 19-18789306-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789306G>C , CM000681.2:g.18789306G>C GRCh38
NC_000019.9:g.18900115G>C , CM000681.1:g.18900115G>C GRCh37
NC_000019.8:g.18761115G>C NCBI36
NG_007070.1:g.7000C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.391-9C>G MANE Select ENSP00000222271.2:n.391-9C>G
ENST00000222271.6:c.391-9C>G ENSP00000222271.2:n.391-9C>G
ENST00000425807.1:c.391-414C>G ENSP00000403792.1:n.391-414C>G
ENST00000542601.6:c.292-9C>G ENSP00000439156.2:n.292-9C>G
NM_000095.2:c.391-9C>G NP_000086.2:n.391-9C>G
NM_000095.3:c.391-9C>G MANE Select NP_000086.2:n.391-9C>G
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