Canonical Allele Identifier: CA581667441
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1411009942
gnomAD v2: 8-48872901-GT-G
gnomAD v3: 8-47960341-GT-G
gnomAD v4: 8-47960341-GT-G
MyVariant Identifiers: chr8:g.48872902del (hg19) chr8:g.47960342del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960342del , CM000670.2:g.47960342del GRCh38
NC_000008.10:g.48872902del , CM000670.1:g.48872902del GRCh37
NC_000008.9:g.49035455del NCBI36
NG_023435.1:g.4842del , LRG_162:g.4842del
NG_032967.1:g.5140del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+22del ENSP00000430329.1:n.-15+22del
NM_005914.3:c.-803del NP_005905.2:n.-803del
NM_182746.2:c.-687del NP_877423.1:n.-687del
XM_005251234.1:c.-1049del XP_005251291.1:n.-1049del
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