Canonical Allele Identifier: CA662490608
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1454319383
gnomAD v3: 10-17849915-G-GA
gnomAD v4: 10-17849915-G-GA
MyVariant Identifiers: chr10:g.17849915_17849916insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849919dup , CM000672.2:g.17849919dup GRCh38
NG_047011.1:g.45577dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+155dup MANE Select ENSP00000455897.1:n.1249+155dup
ENST00000569591.2:c.1249+155dup ENSP00000455897.1:n.1249+155dup
NM_002438.3:c.1249+155dup NP_002429.1:n.1249+155dup
NM_002438.4:c.1249+155dup MANE Select NP_002429.1:n.1249+155dup
Search 100 bp 5'
Search 100 bp 3'