Canonical Allele Identifier: CA2687209623
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960332-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960332G>A , CM000670.2:g.47960332G>A GRCh38
NC_000008.10:g.48872892G>A , CM000670.1:g.48872892G>A GRCh37
NC_000008.9:g.49035445G>A NCBI36
NG_023435.1:g.4852C>T , LRG_162:g.4852C>T
NG_032967.1:g.5130G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+12G>A ENSP00000430329.1:n.-15+12G>A
NM_005914.3:c.-813G>A NP_005905.2:n.-813G>A
NM_182746.2:c.-697G>A NP_877423.1:n.-697G>A
XM_005251234.1:c.-1059G>A XP_005251291.1:n.-1059G>A
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