Canonical Allele Identifier: CA460611293
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1388825161
gnomAD v2: 8-48872873-CTGCGGAGGTAGT-C
gnomAD v3: 8-47960313-CTGCGGAGGTAGT-C
gnomAD v4: 8-47960313-CTGCGGAGGTAGT-C
MyVariant Identifiers: chr8:g.48872874_48872885del (hg19) chr8:g.47960314_47960325del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960315_47960326del , CM000670.2:g.47960315_47960326del GRCh38
NC_000008.10:g.48872875_48872886del , CM000670.1:g.48872875_48872886del GRCh37
NC_000008.9:g.49035428_49035439del NCBI36
NG_023435.1:g.4859_4870del , LRG_162:g.4859_4870del
NG_032967.1:g.5113_5124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-20_-15+6del
NM_005914.3:c.-830_-819del NP_005905.2:n.-830_-819del
NM_182746.2:c.-714_-703del NP_877423.1:n.-714_-703del
XM_005251234.1:c.-1076_-1065del XP_005251291.1:n.-1076_-1065del
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