Canonical Allele Identifier: CA306253831

Gene: COMP

Linked Data

• dbSNP Id: rs913169605
• gnomAD v2: 19-18895970-A-C
• gnomAD v3: 19-18785160-A-C
• gnomAD v4: 19-18785160-A-C
• MyVariant Identifiers: chr19:g.18895970A>C (hg19) ; chr19:g.18785160A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785160A>C , CM000681.2:g.18785160A>C	GRCh38
NC_000019.9:g.18895970A>C , CM000681.1:g.18895970A>C	GRCh37
NC_000019.8:g.18756970A>C	NCBI36
NG_007070.1:g.11145T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1718-68T>G MANE Select	ENSP00000222271.2:n.1718-68T>G
ENST00000222271.6:c.1718-68T>G	ENSP00000222271.2:n.1718-68T>G
ENST00000425807.1:c.1559-68T>G	ENSP00000403792.1:n.1559-68T>G
ENST00000542601.6:c.1619-68T>G	ENSP00000439156.2:n.1619-68T>G
NM_000095.2:c.1718-68T>G	NP_000086.2:n.1718-68T>G
NM_000095.3:c.1718-68T>G MANE Select	NP_000086.2:n.1718-68T>G