Canonical Allele Identifier: CA852595471
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1554648453
gnomAD v3: 8-47960424-T-TA
gnomAD v4: 8-47960424-T-TA
MyVariant Identifiers: chr8:g.48872984_48872985insA (hg19) chr8:g.47960424_47960425insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960430dup , CM000670.2:g.47960430dup GRCh38
NC_000008.10:g.48872990dup , CM000670.1:g.48872990dup GRCh37
NC_000008.9:g.49035543dup NCBI36
NG_023435.1:g.4759dup , LRG_162:g.4759dup
NG_032967.1:g.5228dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+110dup ENSP00000430329.1:n.-15+110dup
NM_005914.3:c.-715dup NP_005905.2:n.-715dup
NM_182746.2:c.-599dup NP_877423.1:n.-599dup
XM_005251234.1:c.-961dup XP_005251291.1:n.-961dup
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