Canonical Allele Identifier: CA506052337
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18895718G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784908G>A , CM000681.2:g.18784908G>A GRCh38
NC_000019.9:g.18895718G>A , CM000681.1:g.18895718G>A GRCh37
NC_000019.8:g.18756718G>A NCBI36
NG_007070.1:g.11397C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1902C>T MANE Select ENSP00000222271.2:p.Gly634=
ENST00000222271.6:c.1902C>T ENSP00000222271.2:p.Gly634=
ENST00000425807.1:c.1743C>T ENSP00000403792.1:p.Gly581=
ENST00000542601.6:c.1803C>T ENSP00000439156.2:p.Gly601=
NM_000095.2:c.1902C>T NP_000086.2:p.Gly634=
NM_000095.3:c.1902C>T MANE Select NP_000086.2:p.Gly634=
Search 100 bp 5'
Search 100 bp 3'