Canonical Allele Identifier: CA1781909371
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1370303429

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960480T>C , CM000670.2:g.47960480T>C GRCh38
NC_000008.10:g.48873040T>C , CM000670.1:g.48873040T>C GRCh37
NC_000008.9:g.49035593T>C NCBI36
NG_023435.1:g.4704A>G , LRG_162:g.4704A>G
NG_032967.1:g.5278T>C

Transcript Alleles

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