Canonical Allele Identifier: CA1781909306
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090796768
gnomAD v4: 8-47960393-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960393C>A , CM000670.2:g.47960393C>A GRCh38
NC_000008.10:g.48872953C>A , CM000670.1:g.48872953C>A GRCh37
NC_000008.9:g.49035506C>A NCBI36
NG_023435.1:g.4791G>T , LRG_162:g.4791G>T
NG_032967.1:g.5191C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+73C>A ENSP00000430329.1:n.-15+73C>A
NM_005914.3:c.-752C>A NP_005905.2:n.-752C>A
NM_182746.2:c.-636C>A NP_877423.1:n.-636C>A
XM_005251234.1:c.-998C>A XP_005251291.1:n.-998C>A
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