Canonical Allele Identifier: CA404896428
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18900044G>C (hg19) chr19:g.18789235G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789235G>C , CM000681.2:g.18789235G>C GRCh38
NC_000019.9:g.18900044G>C , CM000681.1:g.18900044G>C GRCh37
NC_000019.8:g.18761044G>C NCBI36
NG_007070.1:g.7071C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.453C>G MANE Select ENSP00000222271.2:p.Cys151Trp
ENST00000222271.6:c.453C>G ENSP00000222271.2:p.Cys151Trp
ENST00000425807.1:c.391-343C>G ENSP00000403792.1:n.391-343C>G
ENST00000542601.6:c.354C>G ENSP00000439156.2:p.Cys118Trp
NM_000095.2:c.453C>G NP_000086.2:p.Cys151Trp
NM_000095.3:c.453C>G MANE Select NP_000086.2:p.Cys151Trp
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