Canonical Allele Identifier: CA1113556036
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090795005
gnomAD v3: 8-47960297-A-C
gnomAD v4: 8-47960297-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960297A>C , CM000670.2:g.47960297A>C GRCh38
NC_000008.10:g.48872857A>C , CM000670.1:g.48872857A>C GRCh37
NC_000008.9:g.49035410A>C NCBI36
NG_023435.1:g.4887T>G , LRG_162:g.4887T>G
NG_032967.1:g.5095A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-38A>C ENSP00000430329.1:n.-38A>C
NM_005914.3:c.-848A>C NP_005905.2:n.-848A>C
NM_182746.2:c.-732A>C NP_877423.1:n.-732A>C
XM_005251234.1:c.-1094A>C XP_005251291.1:n.-1094A>C
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