Canonical Allele Identifier: CA1781909333
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1294426374
gnomAD v4: 8-47960432-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960432G>T , CM000670.2:g.47960432G>T GRCh38
NC_000008.10:g.48872992G>T , CM000670.1:g.48872992G>T GRCh37
NC_000008.9:g.49035545G>T NCBI36
NG_023435.1:g.4752C>A , LRG_162:g.4752C>A
NG_032967.1:g.5230G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+112G>T ENSP00000430329.1:n.-15+112G>T
NM_005914.3:c.-713G>T NP_005905.2:n.-713G>T
NM_182746.2:c.-597G>T NP_877423.1:n.-597G>T
XM_005251234.1:c.-959G>T XP_005251291.1:n.-959G>T