Canonical Allele Identifier: CA1781909181
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090792599

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960224T>C , CM000670.2:g.47960224T>C GRCh38
NC_000008.10:g.48872784T>C , CM000670.1:g.48872784T>C GRCh37
NC_000008.9:g.49035337T>C NCBI36
NG_023435.1:g.4960A>G , LRG_162:g.4960A>G
NG_032967.1:g.5022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-111T>C ENSP00000430329.1:n.-111T>C
NM_005914.3:c.-921T>C NP_005905.2:n.-921T>C
NM_182746.2:c.-805T>C NP_877423.1:n.-805T>C