Canonical Allele Identifier: CA404885058
Gene: COMP HGNC NCBI

Linked Data

gnomAD v4: 19-18786109-G-C
MyVariant Identifiers: chr19:g.18896919G>C (hg19) chr19:g.18786109G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786109G>C , CM000681.2:g.18786109G>C GRCh38
NC_000019.9:g.18896919G>C , CM000681.1:g.18896919G>C GRCh37
NC_000019.8:g.18757919G>C NCBI36
NG_007070.1:g.10196C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1345C>G MANE Select ENSP00000222271.2:p.Pro449Ala
ENST00000222271.6:c.1345C>G ENSP00000222271.2:p.Pro449Ala
ENST00000425807.1:c.1186C>G ENSP00000403792.1:p.Pro396Ala
ENST00000542601.6:c.1246C>G ENSP00000439156.2:p.Pro416Ala
NM_000095.2:c.1345C>G NP_000086.2:p.Pro449Ala
NM_000095.3:c.1345C>G MANE Select NP_000086.2:p.Pro449Ala
Search 100 bp 5'
Search 100 bp 3'