Canonical Allele Identifier: CA2583622041
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786152G>C , CM000681.2:g.18786152G>C GRCh38
NC_000019.9:g.18896962G>C , CM000681.1:g.18896962G>C GRCh37
NC_000019.8:g.18757962G>C NCBI36
NG_007070.1:g.10153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-6C>G MANE Select ENSP00000222271.2:n.1308-6C>G
ENST00000222271.6:c.1308-6C>G ENSP00000222271.2:n.1308-6C>G
ENST00000425807.1:c.1149-6C>G ENSP00000403792.1:n.1149-6C>G
ENST00000542601.6:c.1209-6C>G ENSP00000439156.2:n.1209-6C>G
ENST00000612179.1:n.558-6C>G
NM_000095.2:c.1308-6C>G NP_000086.2:n.1308-6C>G
NM_000095.3:c.1308-6C>G MANE Select NP_000086.2:n.1308-6C>G