Canonical Allele Identifier: CA176153973
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1038456480
MyVariant Identifiers: chr8:g.48872860A>G (hg19) chr8:g.47960300A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960300A>G , CM000670.2:g.47960300A>G GRCh38
NC_000008.10:g.48872860A>G , CM000670.1:g.48872860A>G GRCh37
NC_000008.9:g.49035413A>G NCBI36
NG_023435.1:g.4884T>C , LRG_162:g.4884T>C
NG_032967.1:g.5098A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-35A>G ENSP00000430329.1:n.-35A>G
NM_005914.3:c.-845A>G NP_005905.2:n.-845A>G
NM_182746.2:c.-729A>G NP_877423.1:n.-729A>G
XM_005251234.1:c.-1091A>G XP_005251291.1:n.-1091A>G
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