Canonical Allele Identifier: CA581667466
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1427322365
gnomAD v2: 8-48873021-G-GC
gnomAD v3: 8-47960461-G-GC
gnomAD v4: 8-47960461-G-GC
MyVariant Identifiers: chr8:g.48873021_48873022insC (hg19) chr8:g.47960461_47960462insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960463dup , CM000670.2:g.47960463dup GRCh38
NC_000008.10:g.48873023dup , CM000670.1:g.48873023dup GRCh37
NC_000008.9:g.49035576dup NCBI36
NG_023435.1:g.4722dup , LRG_162:g.4722dup
NG_032967.1:g.5261dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+143dup ENSP00000430329.1:n.-15+143dup
NM_005914.3:c.-682dup NP_005905.2:n.-682dup
NM_182746.2:c.-566dup NP_877423.1:n.-566dup
XM_005251234.1:c.-928dup XP_005251291.1:n.-928dup
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