Canonical Allele Identifier: CA1781909307
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090796813
gnomAD v4: 8-47960394-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960394T>A , CM000670.2:g.47960394T>A GRCh38
NC_000008.10:g.48872954T>A , CM000670.1:g.48872954T>A GRCh37
NC_000008.9:g.49035507T>A NCBI36
NG_023435.1:g.4790A>T , LRG_162:g.4790A>T
NG_032967.1:g.5192T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+74T>A ENSP00000430329.1:n.-15+74T>A
NM_005914.3:c.-751T>A NP_005905.2:n.-751T>A
NM_182746.2:c.-635T>A NP_877423.1:n.-635T>A
XM_005251234.1:c.-997T>A XP_005251291.1:n.-997T>A