Canonical Allele Identifier: CA506117236

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896651C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785841C>A , CM000681.2:g.18785841C>A	GRCh38
NC_000019.9:g.18896651C>A , CM000681.1:g.18896651C>A	GRCh37
NC_000019.8:g.18757651C>A	NCBI36
NG_007070.1:g.10464G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1500G>T MANE Select	ENSP00000222271.2:p.Val500=
ENST00000222271.6:c.1500G>T	ENSP00000222271.2:p.Val500=
ENST00000425807.1:c.1341G>T	ENSP00000403792.1:p.Val447=
ENST00000542601.6:c.1401G>T	ENSP00000439156.2:p.Val467=
NM_000095.2:c.1500G>T	NP_000086.2:p.Val500=
NM_000095.3:c.1500G>T MANE Select	NP_000086.2:p.Val500=