Canonical Allele Identifier: CA1781909343
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs886062968

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960444C>G , CM000670.2:g.47960444C>G GRCh38
NC_000008.10:g.48873004C>G , CM000670.1:g.48873004C>G GRCh37
NC_000008.9:g.49035557C>G NCBI36
NG_023435.1:g.4740G>C , LRG_162:g.4740G>C
NG_032967.1:g.5242C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+124C>G ENSP00000430329.1:n.-15+124C>G
NM_005914.3:c.-701C>G NP_005905.2:n.-701C>G
NM_182746.2:c.-585C>G NP_877423.1:n.-585C>G
XM_005251234.1:c.-947C>G XP_005251291.1:n.-947C>G