Canonical Allele Identifier: CA1113555988
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090792843
gnomAD v3: 8-47960233-G-T
gnomAD v4: 8-47960233-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960233G>T , CM000670.2:g.47960233G>T GRCh38
NC_000008.10:g.48872793G>T , CM000670.1:g.48872793G>T GRCh37
NC_000008.9:g.49035346G>T NCBI36
NG_023435.1:g.4951C>A , LRG_162:g.4951C>A
NG_032967.1:g.5031G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-102G>T ENSP00000430329.1:n.-102G>T
NM_005914.3:c.-912G>T NP_005905.2:n.-912G>T
NM_182746.2:c.-796G>T NP_877423.1:n.-796G>T
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