Canonical Allele Identifier: CA10651666
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 328607
ClinVar RCV Id: RCV000270982 RCV000365546 RCV001558753
dbSNP Id: rs9407
gnomAD v2: 19-18893633-C-T
gnomAD v3: 19-18782823-C-T
gnomAD v4: 19-18782823-C-T
MyVariant Identifiers: chr19:g.18893633C>T (hg19) chr19:g.18782823C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18782823C>T , CM000681.2:g.18782823C>T GRCh38
NC_000019.9:g.18893633C>T , CM000681.1:g.18893633C>T GRCh37
NC_000019.8:g.18754633C>T NCBI36
NG_007070.1:g.13482G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.*92G>A MANE Select ENSP00000222271.2:n.*92G>A
ENST00000222271.6:c.*92G>A ENSP00000222271.2:n.*92G>A
ENST00000425807.1:c.*92G>A ENSP00000403792.1:n.*92G>A
ENST00000542601.6:c.*92G>A ENSP00000439156.2:n.*92G>A
NM_000095.2:c.*92G>A NP_000086.2:n.*92G>A
NM_000095.3:c.*92G>A MANE Select NP_000086.2:n.*92G>A
Search 100 bp 5'
Search 100 bp 3'