Canonical Allele Identifier: CA404890520
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18898457G>C (hg19) chr19:g.18787648G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787648G>C , CM000681.2:g.18787648G>C GRCh38
NC_000019.9:g.18898457G>C , CM000681.1:g.18898457G>C GRCh37
NC_000019.8:g.18759457G>C NCBI36
NG_007070.1:g.8658C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.978C>G MANE Select ENSP00000222271.2:p.Asp326Glu
ENST00000222271.6:c.978C>G ENSP00000222271.2:p.Asp326Glu
ENST00000425807.1:c.819C>G ENSP00000403792.1:p.Asp273Glu
ENST00000542601.6:c.879C>G ENSP00000439156.2:p.Asp293Glu
NM_000095.2:c.978C>G NP_000086.2:p.Asp326Glu
NM_000095.3:c.978C>G MANE Select NP_000086.2:p.Asp326Glu
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