Canonical Allele Identifier: CA1781909258
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960301A= , CM000670.2:g.47960301A= GRCh38
NC_000008.10:g.48872861A= , CM000670.1:g.48872861A= GRCh37
NC_000008.9:g.49035414A= NCBI36
NG_023435.1:g.4883T= , LRG_162:g.4883T=
NG_032967.1:g.5099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-34A= ENSP00000430329.1:n.-34A=
NM_005914.3:c.-844A= NP_005905.2:n.-844A=
NM_182746.2:c.-728A= NP_877423.1:n.-728A=
XM_005251234.1:c.-1090A= XP_005251291.1:n.-1090A=