Canonical Allele Identifier: CA1781909316
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960405T= , CM000670.2:g.47960405T= GRCh38
NC_000008.10:g.48872965T= , CM000670.1:g.48872965T= GRCh37
NC_000008.9:g.49035518T= NCBI36
NG_023435.1:g.4779A= , LRG_162:g.4779A=
NG_032967.1:g.5203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+85T= ENSP00000430329.1:n.-15+85T=
NM_005914.3:c.-740T= NP_005905.2:n.-740T=
NM_182746.2:c.-624T= NP_877423.1:n.-624T=
XM_005251234.1:c.-986T= XP_005251291.1:n.-986T=