Canonical Allele Identifier: CA1781909320
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090797126
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960419C>A , CM000670.2:g.47960419C>A GRCh38
NC_000008.10:g.48872979C>A , CM000670.1:g.48872979C>A GRCh37
NC_000008.9:g.49035532C>A NCBI36
NG_023435.1:g.4765G>T , LRG_162:g.4765G>T
NG_032967.1:g.5217C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+99C>A ENSP00000430329.1:n.-15+99C>A
NM_005914.3:c.-726C>A NP_005905.2:n.-726C>A
NM_182746.2:c.-610C>A NP_877423.1:n.-610C>A
XM_005251234.1:c.-972C>A XP_005251291.1:n.-972C>A
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