Canonical Allele Identifier: CA581667419
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1267671946
gnomAD v2: 8-48872801-CG-C
gnomAD v3: 8-47960241-CG-C
gnomAD v4: 8-47960241-CG-C
MyVariant Identifiers: chr8:g.48872802del (hg19) chr8:g.47960242del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960244del , CM000670.2:g.47960244del GRCh38
NC_000008.10:g.48872804del , CM000670.1:g.48872804del GRCh37
NC_000008.9:g.49035357del NCBI36
NG_023435.1:g.4942del , LRG_162:g.4942del
NG_032967.1:g.5042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-91del ENSP00000430329.1:n.-91del
NM_005914.3:c.-901del NP_005905.2:n.-901del
NM_182746.2:c.-785del NP_877423.1:n.-785del
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