Canonical Allele Identifier: CA581667421

Gene: MCM4

Linked Data

• dbSNP Id: rs1179476973
• gnomAD v2: 8-48872825-GCCTCT-G
• gnomAD v3: 8-47960265-GCCTCT-G
• gnomAD v4: 8-47960265-GCCTCT-G
• MyVariant Identifiers: chr8:g.48872826_48872830del (hg19) ; chr8:g.47960266_47960270del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47960266_47960270del , CM000670.2:g.47960266_47960270del	GRCh38
NC_000008.10:g.48872826_48872830del , CM000670.1:g.48872826_48872830del	GRCh37
NC_000008.9:g.49035379_49035383del	NCBI36
NG_023435.1:g.4914_4918del , LRG_162:g.4914_4918del
NG_032967.1:g.5064_5068del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518221.5:c.-69_-65del	ENSP00000430329.1:n.-69_-65del
NM_005914.3:c.-879_-875del	NP_005905.2:n.-879_-875del
NM_182746.2:c.-763_-759del	NP_877423.1:n.-763_-759del
XM_005251234.1:c.-1125_-1121del	XP_005251291.1:n.-1125_-1121del