Canonical Allele Identifier: CA506053418

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900080T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789271T>G , CM000681.2:g.18789271T>G	GRCh38
NC_000019.9:g.18900080T>G , CM000681.1:g.18900080T>G	GRCh37
NC_000019.8:g.18761080T>G	NCBI36
NG_007070.1:g.7035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.417A>C MANE Select	ENSP00000222271.2:p.Arg139=
ENST00000222271.6:c.417A>C	ENSP00000222271.2:p.Arg139=
ENST00000425807.1:c.391-379A>C	ENSP00000403792.1:n.391-379A>C
ENST00000542601.6:c.318A>C	ENSP00000439156.2:p.Arg106=
NM_000095.2:c.417A>C	NP_000086.2:p.Arg139=
NM_000095.3:c.417A>C MANE Select	NP_000086.2:p.Arg139=