Canonical Allele Identifier: CA404878168
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1203975764
gnomAD v2: 19-18895781-C-T
gnomAD v4: 19-18784971-C-T
MyVariant Identifiers: chr19:g.18895781C>T (hg19) chr19:g.18784971C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784971C>T , CM000681.2:g.18784971C>T GRCh38
NC_000019.9:g.18895781C>T , CM000681.1:g.18895781C>T GRCh37
NC_000019.8:g.18756781C>T NCBI36
NG_007070.1:g.11334G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1839G>A MANE Select ENSP00000222271.2:p.Met613Ile
ENST00000222271.6:c.1839G>A ENSP00000222271.2:p.Met613Ile
ENST00000425807.1:c.1680G>A ENSP00000403792.1:p.Met560Ile
ENST00000542601.6:c.1740G>A ENSP00000439156.2:p.Met580Ile
NM_000095.2:c.1839G>A NP_000086.2:p.Met613Ile
NM_000095.3:c.1839G>A MANE Select NP_000086.2:p.Met613Ile
Search 100 bp 5'
Search 100 bp 3'