Canonical Allele Identifier: CA176153943
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs978698129
MyVariant Identifiers: chr8:g.48872826_48872828del (hg19) chr8:g.47960266_47960268del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960267_47960269del , CM000670.2:g.47960267_47960269del GRCh38
NC_000008.10:g.48872827_48872829del , CM000670.1:g.48872827_48872829del GRCh37
NC_000008.9:g.49035380_49035382del NCBI36
NG_023435.1:g.4916_4918del , LRG_162:g.4916_4918del
NG_032967.1:g.5065_5067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-68_-66del ENSP00000430329.1:n.-68_-66del
NM_005914.3:c.-878_-876del NP_005905.2:n.-878_-876del
NM_182746.2:c.-762_-760del NP_877423.1:n.-762_-760del
XM_005251234.1:c.-1124_-1122del XP_005251291.1:n.-1124_-1122del
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