Canonical Allele Identifier: CA1113556094
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1589824484
gnomAD v3: 8-47960405-T-C
gnomAD v4: 8-47960405-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960405T>C , CM000670.2:g.47960405T>C GRCh38
NC_000008.10:g.48872965T>C , CM000670.1:g.48872965T>C GRCh37
NC_000008.9:g.49035518T>C NCBI36
NG_023435.1:g.4779A>G , LRG_162:g.4779A>G
NG_032967.1:g.5203T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+85T>C ENSP00000430329.1:n.-15+85T>C
NM_005914.3:c.-740T>C NP_005905.2:n.-740T>C
NM_182746.2:c.-624T>C NP_877423.1:n.-624T>C
XM_005251234.1:c.-986T>C XP_005251291.1:n.-986T>C
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