Canonical Allele Identifier: CA852595357
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1456056447
gnomAD v4: 8-47960290-A-G
MyVariant Identifiers: chr8:g.48872850A>G (hg19) chr8:g.47960290A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960290A>G , CM000670.2:g.47960290A>G GRCh38
NC_000008.10:g.48872850A>G , CM000670.1:g.48872850A>G GRCh37
NC_000008.9:g.49035403A>G NCBI36
NG_023435.1:g.4894T>C , LRG_162:g.4894T>C
NG_032967.1:g.5088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-45A>G ENSP00000430329.1:n.-45A>G
NM_005914.3:c.-855A>G NP_005905.2:n.-855A>G
NM_182746.2:c.-739A>G NP_877423.1:n.-739A>G
XM_005251234.1:c.-1101A>G XP_005251291.1:n.-1101A>G
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