Canonical Allele Identifier: CA852595317
Gene: MCM4 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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