Canonical Allele Identifier: CA1781909184
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090792688
gnomAD v4: 8-47960229-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960229C>T , CM000670.2:g.47960229C>T GRCh38
NC_000008.10:g.48872789C>T , CM000670.1:g.48872789C>T GRCh37
NC_000008.9:g.49035342C>T NCBI36
NG_023435.1:g.4955G>A , LRG_162:g.4955G>A
NG_032967.1:g.5027C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-106C>T ENSP00000430329.1:n.-106C>T
NM_005914.3:c.-916C>T NP_005905.2:n.-916C>T
NM_182746.2:c.-800C>T NP_877423.1:n.-800C>T
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