Canonical Allele Identifier: CA9316441
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs774266370
ExAC: 19:18896951 C / G
gnomAD v2: 19-18896951-C-G
gnomAD v4: 19-18786141-C-G
MyVariant Identifiers: chr19:g.18896951C>G (hg19) chr19:g.18786141C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786141C>G , CM000681.2:g.18786141C>G GRCh38
NC_000019.9:g.18896951C>G , CM000681.1:g.18896951C>G GRCh37
NC_000019.8:g.18757951C>G NCBI36
NG_007070.1:g.10164G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1313G>C MANE Select ENSP00000222271.2:p.Gly438Ala
ENST00000222271.6:c.1313G>C ENSP00000222271.2:p.Gly438Ala
ENST00000425807.1:c.1154G>C ENSP00000403792.1:p.Gly385Ala
ENST00000542601.6:c.1214G>C ENSP00000439156.2:p.Gly405Ala
ENST00000612179.1:n.563G>C
NM_000095.2:c.1313G>C NP_000086.2:p.Gly438Ala
NM_000095.3:c.1313G>C MANE Select NP_000086.2:p.Gly438Ala
Search 100 bp 5'
Search 100 bp 3'