Canonical Allele Identifier: CA1781909281
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960342T= , CM000670.2:g.47960342T= GRCh38
NC_000008.10:g.48872902T= , CM000670.1:g.48872902T= GRCh37
NC_000008.9:g.49035455T= NCBI36
NG_023435.1:g.4842A= , LRG_162:g.4842A=
NG_032967.1:g.5140T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+22T= ENSP00000430329.1:n.-15+22T=
NM_005914.3:c.-803T= NP_005905.2:n.-803T=
NM_182746.2:c.-687T= NP_877423.1:n.-687T=
XM_005251234.1:c.-1049T= XP_005251291.1:n.-1049T=