Canonical Allele Identifier: CA1781909213
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960257G= , CM000670.2:g.47960257G= GRCh38
NC_000008.10:g.48872817G= , CM000670.1:g.48872817G= GRCh37
NC_000008.9:g.49035370G= NCBI36
NG_023435.1:g.4927C= , LRG_162:g.4927C=
NG_032967.1:g.5055G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-78G= ENSP00000430329.1:n.-78G=
NM_005914.3:c.-888G= NP_005905.2:n.-888G=
NM_182746.2:c.-772G= NP_877423.1:n.-772G=
XM_005251234.1:c.-1134G= XP_005251291.1:n.-1134G=