Canonical Allele Identifier: CA1781909352
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960452G= , CM000670.2:g.47960452G= GRCh38
NC_000008.10:g.48873012G= , CM000670.1:g.48873012G= GRCh37
NC_000008.9:g.49035565G= NCBI36
NG_023435.1:g.4732C= , LRG_162:g.4732C=
NG_032967.1:g.5250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+132G= ENSP00000430329.1:n.-15+132G=
NM_005914.3:c.-693G= NP_005905.2:n.-693G=
NM_182746.2:c.-577G= NP_877423.1:n.-577G=
XM_005251234.1:c.-939G= XP_005251291.1:n.-939G=