Canonical Allele Identifier: CA404874877

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18893862A>C (hg19) ; chr19:g.18783052A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18783052A>C , CM000681.2:g.18783052A>C	GRCh38
NC_000019.9:g.18893862A>C , CM000681.1:g.18893862A>C	GRCh37
NC_000019.8:g.18754862A>C	NCBI36
NG_007070.1:g.13253T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.2227+2T>G MANE Select	ENSP00000222271.2:n.2227+2T>G
ENST00000222271.6:c.2227+2T>G	ENSP00000222271.2:n.2227+2T>G
ENST00000425807.1:c.2068+2T>G	ENSP00000403792.1:n.2068+2T>G
ENST00000542601.6:c.2128+2T>G	ENSP00000439156.2:n.2128+2T>G
NM_000095.2:c.2227+2T>G	NP_000086.2:n.2227+2T>G
NM_000095.3:c.2227+2T>G MANE Select	NP_000086.2:n.2227+2T>G