Canonical Allele Identifier: CA1781909329
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960431C= , CM000670.2:g.47960431C= GRCh38
NC_000008.10:g.48872991C= , CM000670.1:g.48872991C= GRCh37
NC_000008.9:g.49035544C= NCBI36
NG_023435.1:g.4753G= , LRG_162:g.4753G=
NG_032967.1:g.5229C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+111C= ENSP00000430329.1:n.-15+111C=
NM_005914.3:c.-714C= NP_005905.2:n.-714C=
NM_182746.2:c.-598C= NP_877423.1:n.-598C=
XM_005251234.1:c.-960C= XP_005251291.1:n.-960C=