Canonical Allele Identifier: CA662490645
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1165878036
gnomAD v3: 10-17849982-TTC-T
gnomAD v4: 10-17849982-TTC-T
MyVariant Identifiers: chr10:g.17849983_17849984del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849984_17849985del , CM000672.2:g.17849984_17849985del GRCh38
NG_047011.1:g.45642_45643del

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+220_1249+221del MANE Select ENSP00000455897.1:n.1249+220_1249+221del
ENST00000569591.2:c.1249+220_1249+221del ENSP00000455897.1:n.1249+220_1249+221del
NM_002438.3:c.1249+220_1249+221del NP_002429.1:n.1249+220_1249+221del
NM_002438.4:c.1249+220_1249+221del MANE Select NP_002429.1:n.1249+220_1249+221del
Search 100 bp 5'
Search 100 bp 3'