Canonical Allele Identifier: CA1781909209
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090793332
gnomAD v4: 8-47960251-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960251T>C , CM000670.2:g.47960251T>C GRCh38
NC_000008.10:g.48872811T>C , CM000670.1:g.48872811T>C GRCh37
NC_000008.9:g.49035364T>C NCBI36
NG_023435.1:g.4933A>G , LRG_162:g.4933A>G
NG_032967.1:g.5049T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-84T>C ENSP00000430329.1:n.-84T>C
NM_005914.3:c.-894T>C NP_005905.2:n.-894T>C
NM_182746.2:c.-778T>C NP_877423.1:n.-778T>C
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