Canonical Allele Identifier: CA176153980
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs941015043

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960320G>A , CM000670.2:g.47960320G>A GRCh38
NC_000008.10:g.48872880G>A , CM000670.1:g.48872880G>A GRCh37
NC_000008.9:g.49035433G>A NCBI36
NG_023435.1:g.4864C>T , LRG_162:g.4864C>T
NG_032967.1:g.5118G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15G>A ENSP00000430329.1:n.-15G>A
NM_005914.3:c.-825G>A NP_005905.2:n.-825G>A
NM_182746.2:c.-709G>A NP_877423.1:n.-709G>A
XM_005251234.1:c.-1071G>A XP_005251291.1:n.-1071G>A