Canonical Allele Identifier: CA404885911
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18897082A>C (hg19) chr19:g.18786272A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786272A>C , CM000681.2:g.18786272A>C GRCh38
NC_000019.9:g.18897082A>C , CM000681.1:g.18897082A>C GRCh37
NC_000019.8:g.18758082A>C NCBI36
NG_007070.1:g.10033T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1274T>G MANE Select ENSP00000222271.2:p.Phe425Cys
ENST00000222271.6:c.1274T>G ENSP00000222271.2:p.Phe425Cys
ENST00000425807.1:c.1115T>G ENSP00000403792.1:p.Phe372Cys
ENST00000542601.6:c.1175T>G ENSP00000439156.2:p.Phe392Cys
ENST00000612179.1:n.524T>G
NM_000095.2:c.1274T>G NP_000086.2:p.Phe425Cys
NM_000095.3:c.1274T>G MANE Select NP_000086.2:p.Phe425Cys
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