Canonical Allele Identifier: CA176153962
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs908565648
gnomAD v4: 8-47960280-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960280A>G , CM000670.2:g.47960280A>G GRCh38
NC_000008.10:g.48872840A>G , CM000670.1:g.48872840A>G GRCh37
NC_000008.9:g.49035393A>G NCBI36
NG_023435.1:g.4904T>C , LRG_162:g.4904T>C
NG_032967.1:g.5078A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-55A>G ENSP00000430329.1:n.-55A>G
NM_005914.3:c.-865A>G NP_005905.2:n.-865A>G
NM_182746.2:c.-749A>G NP_877423.1:n.-749A>G
XM_005251234.1:c.-1111A>G XP_005251291.1:n.-1111A>G