Canonical Allele Identifier: CA2583623246
Gene: COMP HGNC NCBI

Linked Data

gnomAD v4: 19-18789310-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789310G>A , CM000681.2:g.18789310G>A GRCh38
NC_000019.9:g.18900119G>A , CM000681.1:g.18900119G>A GRCh37
NC_000019.8:g.18761119G>A NCBI36
NG_007070.1:g.6996C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.391-13C>T MANE Select ENSP00000222271.2:n.391-13C>T
ENST00000222271.6:c.391-13C>T ENSP00000222271.2:n.391-13C>T
ENST00000425807.1:c.391-418C>T ENSP00000403792.1:n.391-418C>T
ENST00000542601.6:c.292-13C>T ENSP00000439156.2:n.292-13C>T
NM_000095.2:c.391-13C>T NP_000086.2:n.391-13C>T
NM_000095.3:c.391-13C>T MANE Select NP_000086.2:n.391-13C>T
Search 100 bp 5'
Search 100 bp 3'