Canonical Allele Identifier: CA468508632
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1266368025
gnomAD v3: 10-17849939-TATA-T
gnomAD v4: 10-17849939-TATA-T
MyVariant Identifiers: chr10:g.17849940_17849942del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849945_17849947del , CM000672.2:g.17849945_17849947del GRCh38
NG_047011.1:g.45603_45605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+181_1249+183del MANE Select ENSP00000455897.1:n.1249+181_1249+183del
ENST00000569591.2:c.1249+181_1249+183del ENSP00000455897.1:n.1249+181_1249+183del
NM_002438.3:c.1249+181_1249+183del NP_002429.1:n.1249+181_1249+183del
NM_002438.4:c.1249+181_1249+183del MANE Select NP_002429.1:n.1249+181_1249+183del
Search 100 bp 5'
Search 100 bp 3'