Canonical Allele Identifier: CA1781909264
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090795293
gnomAD v4: 8-47960312-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960312C>G , CM000670.2:g.47960312C>G GRCh38
NC_000008.10:g.48872872C>G , CM000670.1:g.48872872C>G GRCh37
NC_000008.9:g.49035425C>G NCBI36
NG_023435.1:g.4872G>C , LRG_162:g.4872G>C
NG_032967.1:g.5110C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-23C>G ENSP00000430329.1:n.-23C>G
NM_005914.3:c.-833C>G NP_005905.2:n.-833C>G
NM_182746.2:c.-717C>G NP_877423.1:n.-717C>G
XM_005251234.1:c.-1079C>G XP_005251291.1:n.-1079C>G