Canonical Allele Identifier: CA1781909327
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090797297

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960425A>T , CM000670.2:g.47960425A>T GRCh38
NC_000008.10:g.48872985A>T , CM000670.1:g.48872985A>T GRCh37
NC_000008.9:g.49035538A>T NCBI36
NG_023435.1:g.4759T>A , LRG_162:g.4759T>A
NG_032967.1:g.5223A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+105A>T ENSP00000430329.1:n.-15+105A>T
NM_005914.3:c.-720A>T NP_005905.2:n.-720A>T
NM_182746.2:c.-604A>T NP_877423.1:n.-604A>T
XM_005251234.1:c.-966A>T XP_005251291.1:n.-966A>T