Canonical Allele Identifier: CA176154001
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs772937275

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960391dup , CM000670.2:g.47960391dup GRCh38
NC_000008.10:g.48872951dup , CM000670.1:g.48872951dup GRCh37
NC_000008.9:g.49035504dup NCBI36
NG_023435.1:g.4796dup , LRG_162:g.4796dup
NG_032967.1:g.5189dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+71dup ENSP00000430329.1:n.-15+71dup
NM_005914.3:c.-754dup NP_005905.2:n.-754dup
NM_182746.2:c.-638dup NP_877423.1:n.-638dup
XM_005251234.1:c.-1000dup XP_005251291.1:n.-1000dup