Canonical Allele Identifier: CA506052741
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896941A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786131A>G , CM000681.2:g.18786131A>G GRCh38
NC_000019.9:g.18896941A>G , CM000681.1:g.18896941A>G GRCh37
NC_000019.8:g.18757941A>G NCBI36
NG_007070.1:g.10174T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1323T>C MANE Select ENSP00000222271.2:p.His441=
ENST00000222271.6:c.1323T>C ENSP00000222271.2:p.His441=
ENST00000425807.1:c.1164T>C ENSP00000403792.1:p.His388=
ENST00000542601.6:c.1224T>C ENSP00000439156.2:p.His408=
ENST00000612179.1:n.573T>C
NM_000095.2:c.1323T>C NP_000086.2:p.His441=
NM_000095.3:c.1323T>C MANE Select NP_000086.2:p.His441=