Canonical Allele Identifier: CA852595323
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1235549762
gnomAD v4: 8-47960255-C-G
MyVariant Identifiers: chr8:g.48872815C>G (hg19) chr8:g.47960255C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960255C>G , CM000670.2:g.47960255C>G GRCh38
NC_000008.10:g.48872815C>G , CM000670.1:g.48872815C>G GRCh37
NC_000008.9:g.49035368C>G NCBI36
NG_023435.1:g.4929G>C , LRG_162:g.4929G>C
NG_032967.1:g.5053C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-80C>G ENSP00000430329.1:n.-80C>G
NM_005914.3:c.-890C>G NP_005905.2:n.-890C>G
NM_182746.2:c.-774C>G NP_877423.1:n.-774C>G
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