Canonical Allele Identifier: CA1781909351
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090798179

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960452_47960459del , CM000670.2:g.47960452_47960459del GRCh38
NC_000008.10:g.48873012_48873019del , CM000670.1:g.48873012_48873019del GRCh37
NC_000008.9:g.49035565_49035572del NCBI36
NG_023435.1:g.4725_4732del , LRG_162:g.4725_4732del
NG_032967.1:g.5250_5257del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+132_-15+139del ENSP00000430329.1:n.-15+132_-15+139del
NM_005914.3:c.-693_-686del NP_005905.2:n.-693_-686del
NM_182746.2:c.-577_-570del NP_877423.1:n.-577_-570del
XM_005251234.1:c.-939_-932del XP_005251291.1:n.-939_-932del