Canonical Allele Identifier: CA404888660
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18898420T>G (hg19) chr19:g.18787611T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787611T>G , CM000681.2:g.18787611T>G GRCh38
NC_000019.9:g.18898420T>G , CM000681.1:g.18898420T>G GRCh37
NC_000019.8:g.18759420T>G NCBI36
NG_007070.1:g.8695A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1015A>C MANE Select ENSP00000222271.2:p.Thr339Pro
ENST00000222271.6:c.1015A>C ENSP00000222271.2:p.Thr339Pro
ENST00000425807.1:c.856A>C ENSP00000403792.1:p.Thr286Pro
ENST00000542601.6:c.916A>C ENSP00000439156.2:p.Thr306Pro
NM_000095.2:c.1015A>C NP_000086.2:p.Thr339Pro
NM_000095.3:c.1015A>C MANE Select NP_000086.2:p.Thr339Pro
Search 100 bp 5'
Search 100 bp 3'