Canonical Allele Identifier: CA1781909332
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960432G= , CM000670.2:g.47960432G= GRCh38
NC_000008.10:g.48872992G= , CM000670.1:g.48872992G= GRCh37
NC_000008.9:g.49035545G= NCBI36
NG_023435.1:g.4752C= , LRG_162:g.4752C=
NG_032967.1:g.5230G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+112G= ENSP00000430329.1:n.-15+112G=
NM_005914.3:c.-713G= NP_005905.2:n.-713G=
NM_182746.2:c.-597G= NP_877423.1:n.-597G=
XM_005251234.1:c.-959G= XP_005251291.1:n.-959G=