Canonical Allele Identifier: CA176153968
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs771934701
gnomAD v3: 8-47960293-C-G
gnomAD v4: 8-47960293-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960293C>G , CM000670.2:g.47960293C>G GRCh38
NC_000008.10:g.48872853C>G , CM000670.1:g.48872853C>G GRCh37
NC_000008.9:g.49035406C>G NCBI36
NG_023435.1:g.4891G>C , LRG_162:g.4891G>C
NG_032967.1:g.5091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-42C>G ENSP00000430329.1:n.-42C>G
NM_005914.3:c.-852C>G NP_005905.2:n.-852C>G
NM_182746.2:c.-736C>G NP_877423.1:n.-736C>G
XM_005251234.1:c.-1098C>G XP_005251291.1:n.-1098C>G