Canonical Allele Identifier: CA1781909218
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090793494
gnomAD v3: 8-47960259-A-G
gnomAD v4: 8-47960259-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960259A>G , CM000670.2:g.47960259A>G GRCh38
NC_000008.10:g.48872819A>G , CM000670.1:g.48872819A>G GRCh37
NC_000008.9:g.49035372A>G NCBI36
NG_023435.1:g.4925T>C , LRG_162:g.4925T>C
NG_032967.1:g.5057A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-76A>G ENSP00000430329.1:n.-76A>G
NM_005914.3:c.-886A>G NP_005905.2:n.-886A>G
NM_182746.2:c.-770A>G NP_877423.1:n.-770A>G
XM_005251234.1:c.-1132A>G XP_005251291.1:n.-1132A>G
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