Canonical Allele Identifier: CA1781909215
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960258T= , CM000670.2:g.47960258T= GRCh38
NC_000008.10:g.48872818T= , CM000670.1:g.48872818T= GRCh37
NC_000008.9:g.49035371T= NCBI36
NG_023435.1:g.4926A= , LRG_162:g.4926A=
NG_032967.1:g.5056T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-77T= ENSP00000430329.1:n.-77T=
NM_005914.3:c.-887T= NP_005905.2:n.-887T=
NM_182746.2:c.-771T= NP_877423.1:n.-771T=
XM_005251234.1:c.-1133T= XP_005251291.1:n.-1133T=