Canonical Allele Identifier: CA9316445
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs765564022
ExAC: 19:18896966 ATAGG / A
gnomAD v2: 19-18896966-ATAGG-A
gnomAD v3: 19-18786156-ATAGG-A
gnomAD v4: 19-18786156-ATAGG-A
MyVariant Identifiers: chr19:g.18896967_18896970del (hg19) chr19:g.18786157_18786160del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786158_18786161del , CM000681.2:g.18786158_18786161del GRCh38
NC_000019.9:g.18896968_18896971del , CM000681.1:g.18896968_18896971del GRCh37
NC_000019.8:g.18757968_18757971del NCBI36
NG_007070.1:g.10145_10148del

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1308-14_1308-11del MANE Select ENSP00000222271.2:n.1308-14_1308-11del
ENST00000222271.6:c.1308-14_1308-11del ENSP00000222271.2:n.1308-14_1308-11del
ENST00000425807.1:c.1149-14_1149-11del ENSP00000403792.1:n.1149-14_1149-11del
ENST00000542601.6:c.1209-14_1209-11del ENSP00000439156.2:n.1209-14_1209-11del
ENST00000612179.1:n.558-14_558-11del
NM_000095.2:c.1308-14_1308-11del NP_000086.2:n.1308-14_1308-11del
NM_000095.3:c.1308-14_1308-11del MANE Select NP_000086.2:n.1308-14_1308-11del
Search 100 bp 5'
Search 100 bp 3'