Canonical Allele Identifier: CA176153999
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs201113487
MyVariant Identifiers: chr8:g.48872933A>T (hg19) chr8:g.47960373A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960373A>T , CM000670.2:g.47960373A>T GRCh38
NC_000008.10:g.48872933A>T , CM000670.1:g.48872933A>T GRCh37
NC_000008.9:g.49035486A>T NCBI36
NG_023435.1:g.4811T>A , LRG_162:g.4811T>A
NG_032967.1:g.5171A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+53A>T ENSP00000430329.1:n.-15+53A>T
NM_005914.3:c.-772A>T NP_005905.2:n.-772A>T
NM_182746.2:c.-656A>T NP_877423.1:n.-656A>T
XM_005251234.1:c.-1018A>T XP_005251291.1:n.-1018A>T
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