Canonical Allele Identifier: CA852595537
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1198721540
gnomAD v4: 8-47960468-G-A
MyVariant Identifiers: chr8:g.48873028G>A (hg19) chr8:g.47960468G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960468G>A , CM000670.2:g.47960468G>A GRCh38
NC_000008.10:g.48873028G>A , CM000670.1:g.48873028G>A GRCh37
NC_000008.9:g.49035581G>A NCBI36
NG_023435.1:g.4716C>T , LRG_162:g.4716C>T
NG_032967.1:g.5266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+148G>A ENSP00000430329.1:n.-15+148G>A
NM_005914.3:c.-677G>A NP_005905.2:n.-677G>A
NM_182746.2:c.-561G>A NP_877423.1:n.-561G>A
XM_005251234.1:c.-923G>A XP_005251291.1:n.-923G>A
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