Canonical Allele Identifier: CA1781909362
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960473A= , CM000670.2:g.47960473A= GRCh38
NC_000008.10:g.48873033A= , CM000670.1:g.48873033A= GRCh37
NC_000008.9:g.49035586A= NCBI36
NG_023435.1:g.4711T= , LRG_162:g.4711T=
NG_032967.1:g.5271A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+153A= ENSP00000430329.1:n.-15+153A=
NM_005914.3:c.-672A= NP_005905.2:n.-672A=
NM_182746.2:c.-556A= NP_877423.1:n.-556A=
XM_005251234.1:c.-918A= XP_005251291.1:n.-918A=