Canonical Allele Identifier: CA1781909369
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090798893

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960480dup , CM000670.2:g.47960480dup GRCh38
NC_000008.10:g.48873040dup , CM000670.1:g.48873040dup GRCh37
NC_000008.9:g.49035593dup NCBI36
NG_023435.1:g.4706dup , LRG_162:g.4706dup
NG_032967.1:g.5278dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+160dup ENSP00000430329.1:n.-15+160dup
NM_005914.3:c.-665dup NP_005905.2:n.-665dup
NM_182746.2:c.-549dup NP_877423.1:n.-549dup
XM_005251234.1:c.-911dup XP_005251291.1:n.-911dup