Canonical Allele Identifier: CA1781909339
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090797688

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960442_47960457del , CM000670.2:g.47960442_47960457del GRCh38
NC_000008.10:g.48873002_48873017del , CM000670.1:g.48873002_48873017del GRCh37
NC_000008.9:g.49035555_49035570del NCBI36
NG_023435.1:g.4728_4743del , LRG_162:g.4728_4743del
NG_032967.1:g.5240_5255del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+122_-15+137del ENSP00000430329.1:n.-15+122_-15+137del
NM_005914.3:c.-703_-688del NP_005905.2:n.-703_-688del
NM_182746.2:c.-587_-572del NP_877423.1:n.-587_-572del
XM_005251234.1:c.-949_-934del XP_005251291.1:n.-949_-934del