Canonical Allele Identifier: CA506052706
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896917G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786107G>C , CM000681.2:g.18786107G>C GRCh38
NC_000019.9:g.18896917G>C , CM000681.1:g.18896917G>C GRCh37
NC_000019.8:g.18757917G>C NCBI36
NG_007070.1:g.10198C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1347C>G MANE Select ENSP00000222271.2:p.Pro449=
ENST00000222271.6:c.1347C>G ENSP00000222271.2:p.Pro449=
ENST00000425807.1:c.1188C>G ENSP00000403792.1:p.Pro396=
ENST00000542601.6:c.1248C>G ENSP00000439156.2:p.Pro416=
NM_000095.2:c.1347C>G NP_000086.2:p.Pro449=
NM_000095.3:c.1347C>G MANE Select NP_000086.2:p.Pro449=