Canonical Allele Identifier: CA852595397
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1433561785
MyVariant Identifiers: chr8:g.48872927del (hg19) chr8:g.47960367del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960367del , CM000670.2:g.47960367del GRCh38
NC_000008.10:g.48872927del , CM000670.1:g.48872927del GRCh37
NC_000008.9:g.49035480del NCBI36
NG_023435.1:g.4817del , LRG_162:g.4817del
NG_032967.1:g.5165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+47del ENSP00000430329.1:n.-15+47del
NM_005914.3:c.-778del NP_005905.2:n.-778del
NM_182746.2:c.-662del NP_877423.1:n.-662del
XM_005251234.1:c.-1024del XP_005251291.1:n.-1024del
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