Canonical Allele Identifier: CA506117342

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896800A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785990A>C , CM000681.2:g.18785990A>C	GRCh38
NC_000019.9:g.18896800A>C , CM000681.1:g.18896800A>C	GRCh37
NC_000019.8:g.18757800A>C	NCBI36
NG_007070.1:g.10315T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1464T>G MANE Select	ENSP00000222271.2:p.Pro488=
ENST00000222271.6:c.1464T>G	ENSP00000222271.2:p.Pro488=
ENST00000425807.1:c.1305T>G	ENSP00000403792.1:p.Pro435=
ENST00000542601.6:c.1365T>G	ENSP00000439156.2:p.Pro455=
NM_000095.2:c.1464T>G	NP_000086.2:p.Pro488=
NM_000095.3:c.1464T>G MANE Select	NP_000086.2:p.Pro488=