Canonical Allele Identifier: CA1781909249
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960295T= , CM000670.2:g.47960295T= GRCh38
NC_000008.10:g.48872855T= , CM000670.1:g.48872855T= GRCh37
NC_000008.9:g.49035408T= NCBI36
NG_023435.1:g.4889A= , LRG_162:g.4889A=
NG_032967.1:g.5093T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-40T= ENSP00000430329.1:n.-40T=
NM_005914.3:c.-850T= NP_005905.2:n.-850T=
NM_182746.2:c.-734T= NP_877423.1:n.-734T=
XM_005251234.1:c.-1096T= XP_005251291.1:n.-1096T=