Canonical Allele Identifier: CA581667463
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1186941745
gnomAD v2: 8-48872986-A-T
gnomAD v3: 8-47960426-A-T
gnomAD v4: 8-47960426-A-T
MyVariant Identifiers: chr8:g.48872986A>T (hg19) chr8:g.47960426A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960426A>T , CM000670.2:g.47960426A>T GRCh38
NC_000008.10:g.48872986A>T , CM000670.1:g.48872986A>T GRCh37
NC_000008.9:g.49035539A>T NCBI36
NG_023435.1:g.4758T>A , LRG_162:g.4758T>A
NG_032967.1:g.5224A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+106A>T ENSP00000430329.1:n.-15+106A>T
NM_005914.3:c.-719A>T NP_005905.2:n.-719A>T
NM_182746.2:c.-603A>T NP_877423.1:n.-603A>T
XM_005251234.1:c.-965A>T XP_005251291.1:n.-965A>T
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