Canonical Allele Identifier: CA404896824
Gene: COMP HGNC NCBI

Linked Data

gnomAD v4: 19-18789299-T-A
MyVariant Identifiers: chr19:g.18900108T>A (hg19) chr19:g.18789299T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789299T>A , CM000681.2:g.18789299T>A GRCh38
NC_000019.9:g.18900108T>A , CM000681.1:g.18900108T>A GRCh37
NC_000019.8:g.18761108T>A NCBI36
NG_007070.1:g.7007A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.391-2A>T MANE Select ENSP00000222271.2:n.391-2A>T
ENST00000222271.6:c.391-2A>T ENSP00000222271.2:n.391-2A>T
ENST00000425807.1:c.391-407A>T ENSP00000403792.1:n.391-407A>T
ENST00000542601.6:c.292-2A>T ENSP00000439156.2:n.292-2A>T
NM_000095.2:c.391-2A>T NP_000086.2:n.391-2A>T
NM_000095.3:c.391-2A>T MANE Select NP_000086.2:n.391-2A>T
Search 100 bp 5'
Search 100 bp 3'