Canonical Allele Identifier: CA10625528
Gene: MCM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 363192
ClinVar RCV Id: RCV000306375
dbSNP Id: rs886062967
gnomAD v3: 8-47960423-A-AT
gnomAD v4: 8-47960423-A-AT
MyVariant Identifiers: chr8:g.48872984dupT (hg19) chr8:g.48872984_48872985insT (hg19) chr8:g.48872983_48872984insT (hg19) chr8:g.47960424dupT (hg38) chr8:g.47960424_47960425insT (hg38) chr8:g.47960423_47960424insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960424dup , CM000670.2:g.47960424dup GRCh38
NC_000008.10:g.48872984dup , CM000670.1:g.48872984dup GRCh37
NC_000008.9:g.49035537dup NCBI36
NG_023435.1:g.4760dup , LRG_162:g.4760dup
NG_032967.1:g.5222dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+104dup ENSP00000430329.1:n.-15+104dup
NM_005914.3:c.-721dup NP_005905.2:n.-721dup
NM_182746.2:c.-605dup NP_877423.1:n.-605dup
XM_005251234.1:c.-967dup XP_005251291.1:n.-967dup
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