Canonical Allele Identifier: CA1781909273
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960325T= , CM000670.2:g.47960325T= GRCh38
NC_000008.10:g.48872885T= , CM000670.1:g.48872885T= GRCh37
NC_000008.9:g.49035438T= NCBI36
NG_023435.1:g.4859A= , LRG_162:g.4859A=
NG_032967.1:g.5123T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+5T= ENSP00000430329.1:n.-15+5T=
NM_005914.3:c.-820T= NP_005905.2:n.-820T=
NM_182746.2:c.-704T= NP_877423.1:n.-704T=
XM_005251234.1:c.-1066T= XP_005251291.1:n.-1066T=