Canonical Allele Identifier: CA1781909364
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960474A= , CM000670.2:g.47960474A= GRCh38
NC_000008.10:g.48873034A= , CM000670.1:g.48873034A= GRCh37
NC_000008.9:g.49035587A= NCBI36
NG_023435.1:g.4710T= , LRG_162:g.4710T=
NG_032967.1:g.5272A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+154A= ENSP00000430329.1:n.-15+154A=
NM_005914.3:c.-671A= NP_005905.2:n.-671A=
NM_182746.2:c.-555A= NP_877423.1:n.-555A=
XM_005251234.1:c.-917A= XP_005251291.1:n.-917A=