Canonical Allele Identifier: CA2326523972
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18783044C= , CM000681.2:g.18783044C= GRCh38
NC_000019.9:g.18893854C= , CM000681.1:g.18893854C= GRCh37
NC_000019.8:g.18754854C= NCBI36
NG_007070.1:g.13261G=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.2227+10G= MANE Select ENSP00000222271.2:n.2227+10G=
ENST00000222271.6:c.2227+10G= ENSP00000222271.2:n.2227+10G=
ENST00000425807.1:c.2068+10G= ENSP00000403792.1:n.2068+10G=
ENST00000542601.6:c.2128+10G= ENSP00000439156.2:n.2128+10G=
NM_000095.2:c.2227+10G= NP_000086.2:n.2227+10G=
NM_000095.3:c.2227+10G= MANE Select NP_000086.2:n.2227+10G=
Search 100 bp 5'
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