Canonical Allele Identifier: CA1781909177
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs745602359

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960220G>C , CM000670.2:g.47960220G>C GRCh38
NC_000008.10:g.48872780G>C , CM000670.1:g.48872780G>C GRCh37
NC_000008.9:g.49035333G>C NCBI36
NG_023435.1:g.4964C>G , LRG_162:g.4964C>G
NG_032967.1:g.5018G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-115G>C ENSP00000430329.1:n.-115G>C
NM_005914.3:c.-925G>C NP_005905.2:n.-925G>C
NM_182746.2:c.-809G>C NP_877423.1:n.-809G>C