Canonical Allele Identifier: CA1781909252
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1589824260
gnomAD v4: 8-47960296-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960296A>G , CM000670.2:g.47960296A>G GRCh38
NC_000008.10:g.48872856A>G , CM000670.1:g.48872856A>G GRCh37
NC_000008.9:g.49035409A>G NCBI36
NG_023435.1:g.4888T>C , LRG_162:g.4888T>C
NG_032967.1:g.5094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-39A>G ENSP00000430329.1:n.-39A>G
NM_005914.3:c.-849A>G NP_005905.2:n.-849A>G
NM_182746.2:c.-733A>G NP_877423.1:n.-733A>G
XM_005251234.1:c.-1095A>G XP_005251291.1:n.-1095A>G