Canonical Allele Identifier: CA1113555982
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090792645
gnomAD v3: 8-47960228-C-T
gnomAD v4: 8-47960228-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960228C>T , CM000670.2:g.47960228C>T GRCh38
NC_000008.10:g.48872788C>T , CM000670.1:g.48872788C>T GRCh37
NC_000008.9:g.49035341C>T NCBI36
NG_023435.1:g.4956G>A , LRG_162:g.4956G>A
NG_032967.1:g.5026C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-107C>T ENSP00000430329.1:n.-107C>T
NM_005914.3:c.-917C>T NP_005905.2:n.-917C>T
NM_182746.2:c.-801C>T NP_877423.1:n.-801C>T
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