Canonical Allele Identifier: CA1781909308
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960394T= , CM000670.2:g.47960394T= GRCh38
NC_000008.10:g.48872954T= , CM000670.1:g.48872954T= GRCh37
NC_000008.9:g.49035507T= NCBI36
NG_023435.1:g.4790A= , LRG_162:g.4790A=
NG_032967.1:g.5192T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+74T= ENSP00000430329.1:n.-15+74T=
NM_005914.3:c.-751T= NP_005905.2:n.-751T=
NM_182746.2:c.-635T= NP_877423.1:n.-635T=
XM_005251234.1:c.-997T= XP_005251291.1:n.-997T=