Canonical Allele Identifier: CA404896600
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18900076G>T (hg19) chr19:g.18789267G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789267G>T , CM000681.2:g.18789267G>T GRCh38
NC_000019.9:g.18900076G>T , CM000681.1:g.18900076G>T GRCh37
NC_000019.8:g.18761076G>T NCBI36
NG_007070.1:g.7039C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.421C>A MANE Select ENSP00000222271.2:p.Arg141Ser
ENST00000222271.6:c.421C>A ENSP00000222271.2:p.Arg141Ser
ENST00000425807.1:c.391-375C>A ENSP00000403792.1:n.391-375C>A
ENST00000542601.6:c.322C>A ENSP00000439156.2:p.Arg108Ser
NM_000095.2:c.421C>A NP_000086.2:p.Arg141Ser
NM_000095.3:c.421C>A MANE Select NP_000086.2:p.Arg141Ser
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