Canonical Allele Identifier: CA10625531
Gene: MCM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 363193
ClinVar RCV Id: RCV000365824
dbSNP Id: rs886062968
gnomAD v4: 8-47960444-C-A
MyVariant Identifiers: chr8:g.48873004C>A (hg19) chr8:g.47960444C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960444C>A , CM000670.2:g.47960444C>A GRCh38
NC_000008.10:g.48873004C>A , CM000670.1:g.48873004C>A GRCh37
NC_000008.9:g.49035557C>A NCBI36
NG_023435.1:g.4740G>T , LRG_162:g.4740G>T
NG_032967.1:g.5242C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+124C>A ENSP00000430329.1:n.-15+124C>A
NM_005914.3:c.-701C>A NP_005905.2:n.-701C>A
NM_182746.2:c.-585C>A NP_877423.1:n.-585C>A
XM_005251234.1:c.-947C>A XP_005251291.1:n.-947C>A
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