Canonical Allele Identifier: CA1781909253
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960297A= , CM000670.2:g.47960297A= GRCh38
NC_000008.10:g.48872857A= , CM000670.1:g.48872857A= GRCh37
NC_000008.9:g.49035410A= NCBI36
NG_023435.1:g.4887T= , LRG_162:g.4887T=
NG_032967.1:g.5095A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-38A= ENSP00000430329.1:n.-38A=
NM_005914.3:c.-848A= NP_005905.2:n.-848A=
NM_182746.2:c.-732A= NP_877423.1:n.-732A=
XM_005251234.1:c.-1094A= XP_005251291.1:n.-1094A=