Canonical Allele Identifier: CA506052354
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18895742G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784932G>C , CM000681.2:g.18784932G>C GRCh38
NC_000019.9:g.18895742G>C , CM000681.1:g.18895742G>C GRCh37
NC_000019.8:g.18756742G>C NCBI36
NG_007070.1:g.11373C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1878C>G MANE Select ENSP00000222271.2:p.Pro626=
ENST00000222271.6:c.1878C>G ENSP00000222271.2:p.Pro626=
ENST00000425807.1:c.1719C>G ENSP00000403792.1:p.Pro573=
ENST00000542601.6:c.1779C>G ENSP00000439156.2:p.Pro593=
NM_000095.2:c.1878C>G NP_000086.2:p.Pro626=
NM_000095.3:c.1878C>G MANE Select NP_000086.2:p.Pro626=
Search 100 bp 5'
Search 100 bp 3'