Canonical Allele Identifier: CA1781909201
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1589824076
gnomAD v4: 8-47960245-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960245A>G , CM000670.2:g.47960245A>G GRCh38
NC_000008.10:g.48872805A>G , CM000670.1:g.48872805A>G GRCh37
NC_000008.9:g.49035358A>G NCBI36
NG_023435.1:g.4939T>C , LRG_162:g.4939T>C
NG_032967.1:g.5043A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-90A>G ENSP00000430329.1:n.-90A>G
NM_005914.3:c.-900A>G NP_005905.2:n.-900A>G
NM_182746.2:c.-784A>G NP_877423.1:n.-784A>G
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