Canonical Allele Identifier: CA852595316
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1177434601
gnomAD v3: 8-47960250-C-A
gnomAD v4: 8-47960250-C-A
MyVariant Identifiers: chr8:g.48872810C>A (hg19) chr8:g.47960250C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960250C>A , CM000670.2:g.47960250C>A GRCh38
NC_000008.10:g.48872810C>A , CM000670.1:g.48872810C>A GRCh37
NC_000008.9:g.49035363C>A NCBI36
NG_023435.1:g.4934G>T , LRG_162:g.4934G>T
NG_032967.1:g.5048C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-85C>A ENSP00000430329.1:n.-85C>A
NM_005914.3:c.-895C>A NP_005905.2:n.-895C>A
NM_182746.2:c.-779C>A NP_877423.1:n.-779C>A
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