Canonical Allele Identifier: CA852595381
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1241618935
MyVariant Identifiers: chr8:g.48872897C>G (hg19) chr8:g.47960337C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960337C>G , CM000670.2:g.47960337C>G GRCh38
NC_000008.10:g.48872897C>G , CM000670.1:g.48872897C>G GRCh37
NC_000008.9:g.49035450C>G NCBI36
NG_023435.1:g.4847G>C , LRG_162:g.4847G>C
NG_032967.1:g.5135C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+17C>G ENSP00000430329.1:n.-15+17C>G
NM_005914.3:c.-808C>G NP_005905.2:n.-808C>G
NM_182746.2:c.-692C>G NP_877423.1:n.-692C>G
XM_005251234.1:c.-1054C>G XP_005251291.1:n.-1054C>G
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