Canonical Allele Identifier: CA1781909262
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090795250
gnomAD v4: 8-47960308-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960308C>T , CM000670.2:g.47960308C>T GRCh38
NC_000008.10:g.48872868C>T , CM000670.1:g.48872868C>T GRCh37
NC_000008.9:g.49035421C>T NCBI36
NG_023435.1:g.4876G>A , LRG_162:g.4876G>A
NG_032967.1:g.5106C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-27C>T ENSP00000430329.1:n.-27C>T
NM_005914.3:c.-837C>T NP_005905.2:n.-837C>T
NM_182746.2:c.-721C>T NP_877423.1:n.-721C>T
XM_005251234.1:c.-1083C>T XP_005251291.1:n.-1083C>T