Canonical Allele Identifier: CA2687209753
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960436-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960436A>C , CM000670.2:g.47960436A>C GRCh38
NC_000008.10:g.48872996A>C , CM000670.1:g.48872996A>C GRCh37
NC_000008.9:g.49035549A>C NCBI36
NG_023435.1:g.4748T>G , LRG_162:g.4748T>G
NG_032967.1:g.5234A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+116A>C ENSP00000430329.1:n.-15+116A>C
NM_005914.3:c.-709A>C NP_005905.2:n.-709A>C
NM_182746.2:c.-593A>C NP_877423.1:n.-593A>C
XM_005251234.1:c.-955A>C XP_005251291.1:n.-955A>C