Canonical Allele Identifier: CA2687209590
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2154504888
gnomAD v4: 8-47960316-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960316C>T , CM000670.2:g.47960316C>T GRCh38
NC_000008.10:g.48872876C>T , CM000670.1:g.48872876C>T GRCh37
NC_000008.9:g.49035429C>T NCBI36
NG_023435.1:g.4868G>A , LRG_162:g.4868G>A
NG_032967.1:g.5114C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-19C>T ENSP00000430329.1:n.-19C>T
NM_005914.3:c.-829C>T NP_005905.2:n.-829C>T
NM_182746.2:c.-713C>T NP_877423.1:n.-713C>T
XM_005251234.1:c.-1075C>T XP_005251291.1:n.-1075C>T