Canonical Allele Identifier: CA581667424
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1472885475
gnomAD v2: 8-48872830-T-TAG
gnomAD v3: 8-47960270-T-TAG
gnomAD v4: 8-47960270-T-TAG
MyVariant Identifiers: chr8:g.48872830_48872831insAG (hg19) chr8:g.47960270_47960271insAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960270_47960271insAG , CM000670.2:g.47960270_47960271insAG GRCh38
NC_000008.10:g.48872830_48872831insAG , CM000670.1:g.48872830_48872831insAG GRCh37
NC_000008.9:g.49035383_49035384insAG NCBI36
NG_023435.1:g.4913_4914insCT , LRG_162:g.4913_4914insCT
NG_032967.1:g.5068_5069insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-65_-64insAG ENSP00000430329.1:n.-65_-64insAG
NM_005914.3:c.-875_-874insAG NP_005905.2:n.-875_-874insAG
NM_182746.2:c.-759_-758insAG NP_877423.1:n.-759_-758insAG
XM_005251234.1:c.-1121_-1120insAG XP_005251291.1:n.-1121_-1120insAG
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