Canonical Allele Identifier: CA404885217
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896940G>C (hg19) chr19:g.18786130G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786130G>C , CM000681.2:g.18786130G>C GRCh38
NC_000019.9:g.18896940G>C , CM000681.1:g.18896940G>C GRCh37
NC_000019.8:g.18757940G>C NCBI36
NG_007070.1:g.10175C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1324C>G MANE Select ENSP00000222271.2:p.Gln442Glu
ENST00000222271.6:c.1324C>G ENSP00000222271.2:p.Gln442Glu
ENST00000425807.1:c.1165C>G ENSP00000403792.1:p.Gln389Glu
ENST00000542601.6:c.1225C>G ENSP00000439156.2:p.Gln409Glu
ENST00000612179.1:n.574C>G
NM_000095.2:c.1324C>G NP_000086.2:p.Gln442Glu
NM_000095.3:c.1324C>G MANE Select NP_000086.2:p.Gln442Glu
Search 100 bp 5'
Search 100 bp 3'