Canonical Allele Identifier: CA2326525622
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786196T= , CM000681.2:g.18786196T= GRCh38
NC_000019.9:g.18897006T= , CM000681.1:g.18897006T= GRCh37
NC_000019.8:g.18758006T= NCBI36
NG_007070.1:g.10109A=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1307+43A= MANE Select ENSP00000222271.2:n.1307+43A=
ENST00000222271.6:c.1307+43A= ENSP00000222271.2:n.1307+43A=
ENST00000425807.1:c.1148+43A= ENSP00000403792.1:n.1148+43A=
ENST00000542601.6:c.1208+43A= ENSP00000439156.2:n.1208+43A=
ENST00000612179.1:n.557+43A=
NM_000095.2:c.1307+43A= NP_000086.2:n.1307+43A=
NM_000095.3:c.1307+43A= MANE Select NP_000086.2:n.1307+43A=
Search 100 bp 5'
Search 100 bp 3'