Canonical Allele Identifier: CA404884101
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1678031
ClinVar RCV Id: RCV002224622
dbSNP Id: rs2145900718
MyVariant Identifiers: chr19:g.18896783T>C (hg19) chr19:g.18785973T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785973T>C , CM000681.2:g.18785973T>C GRCh38
NC_000019.9:g.18896783T>C , CM000681.1:g.18896783T>C GRCh37
NC_000019.8:g.18757783T>C NCBI36
NG_007070.1:g.10332A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1481A>G MANE Select ENSP00000222271.2:p.Asp494Gly
ENST00000222271.6:c.1481A>G ENSP00000222271.2:p.Asp494Gly
ENST00000425807.1:c.1322A>G ENSP00000403792.1:p.Asp441Gly
ENST00000542601.6:c.1382A>G ENSP00000439156.2:p.Asp461Gly
NM_000095.2:c.1481A>G NP_000086.2:p.Asp494Gly
NM_000095.3:c.1481A>G MANE Select NP_000086.2:p.Asp494Gly
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Search 100 bp 3'