Canonical Allele Identifier: CA2687209397
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960222-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960222A>C , CM000670.2:g.47960222A>C GRCh38
NC_000008.10:g.48872782A>C , CM000670.1:g.48872782A>C GRCh37
NC_000008.9:g.49035335A>C NCBI36
NG_023435.1:g.4962T>G , LRG_162:g.4962T>G
NG_032967.1:g.5020A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-113A>C ENSP00000430329.1:n.-113A>C
NM_005914.3:c.-923A>C NP_005905.2:n.-923A>C
NM_182746.2:c.-807A>C NP_877423.1:n.-807A>C
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