Canonical Allele Identifier: CA581667426
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1414236175
gnomAD v2: 8-48872841-TC-T
gnomAD v3: 8-47960281-TC-T
gnomAD v4: 8-47960281-TC-T
MyVariant Identifiers: chr8:g.48872842del (hg19) chr8:g.47960282del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960282del , CM000670.2:g.47960282del GRCh38
NC_000008.10:g.48872842del , CM000670.1:g.48872842del GRCh37
NC_000008.9:g.49035395del NCBI36
NG_023435.1:g.4902del , LRG_162:g.4902del
NG_032967.1:g.5080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-53del ENSP00000430329.1:n.-53del
NM_005914.3:c.-863del NP_005905.2:n.-863del
NM_182746.2:c.-747del NP_877423.1:n.-747del
XM_005251234.1:c.-1109del XP_005251291.1:n.-1109del
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