Canonical Allele Identifier: CA1781909299
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960373A= , CM000670.2:g.47960373A= GRCh38
NC_000008.10:g.48872933A= , CM000670.1:g.48872933A= GRCh37
NC_000008.9:g.49035486A= NCBI36
NG_023435.1:g.4811T= , LRG_162:g.4811T=
NG_032967.1:g.5171A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+53A= ENSP00000430329.1:n.-15+53A=
NM_005914.3:c.-772A= NP_005905.2:n.-772A=
NM_182746.2:c.-656A= NP_877423.1:n.-656A=
XM_005251234.1:c.-1018A= XP_005251291.1:n.-1018A=