Canonical Allele Identifier: CA404896817

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900107C>G (hg19) ; chr19:g.18789298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789298C>G , CM000681.2:g.18789298C>G	GRCh38
NC_000019.9:g.18900107C>G , CM000681.1:g.18900107C>G	GRCh37
NC_000019.8:g.18761107C>G	NCBI36
NG_007070.1:g.7008G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.391-1G>C MANE Select	ENSP00000222271.2:n.391-1G>C
ENST00000222271.6:c.391-1G>C	ENSP00000222271.2:n.391-1G>C
ENST00000425807.1:c.391-406G>C	ENSP00000403792.1:n.391-406G>C
ENST00000542601.6:c.292-1G>C	ENSP00000439156.2:n.292-1G>C
NM_000095.2:c.391-1G>C	NP_000086.2:n.391-1G>C
NM_000095.3:c.391-1G>C MANE Select	NP_000086.2:n.391-1G>C