Canonical Allele Identifier: CA404888725
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18898429G>C (hg19) chr19:g.18787620G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787620G>C , CM000681.2:g.18787620G>C GRCh38
NC_000019.9:g.18898429G>C , CM000681.1:g.18898429G>C GRCh37
NC_000019.8:g.18759429G>C NCBI36
NG_007070.1:g.8686C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1006C>G MANE Select ENSP00000222271.2:p.Gln336Glu
ENST00000222271.6:c.1006C>G ENSP00000222271.2:p.Gln336Glu
ENST00000425807.1:c.847C>G ENSP00000403792.1:p.Gln283Glu
ENST00000542601.6:c.907C>G ENSP00000439156.2:p.Gln303Glu
NM_000095.2:c.1006C>G NP_000086.2:p.Gln336Glu
NM_000095.3:c.1006C>G MANE Select NP_000086.2:p.Gln336Glu
Search 100 bp 5'
Search 100 bp 3'