Canonical Allele Identifier: CA1781909293
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960355T= , CM000670.2:g.47960355T= GRCh38
NC_000008.10:g.48872915T= , CM000670.1:g.48872915T= GRCh37
NC_000008.9:g.49035468T= NCBI36
NG_023435.1:g.4829A= , LRG_162:g.4829A=
NG_032967.1:g.5153T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+35T= ENSP00000430329.1:n.-15+35T=
NM_005914.3:c.-790T= NP_005905.2:n.-790T=
NM_182746.2:c.-674T= NP_877423.1:n.-674T=
XM_005251234.1:c.-1036T= XP_005251291.1:n.-1036T=