Canonical Allele Identifier: CA176153988
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs906427652
gnomAD v3: 8-47960347-G-C
gnomAD v4: 8-47960347-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960347G>C , CM000670.2:g.47960347G>C GRCh38
NC_000008.10:g.48872907G>C , CM000670.1:g.48872907G>C GRCh37
NC_000008.9:g.49035460G>C NCBI36
NG_023435.1:g.4837C>G , LRG_162:g.4837C>G
NG_032967.1:g.5145G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+27G>C ENSP00000430329.1:n.-15+27G>C
NM_005914.3:c.-798G>C NP_005905.2:n.-798G>C
NM_182746.2:c.-682G>C NP_877423.1:n.-682G>C
XM_005251234.1:c.-1044G>C XP_005251291.1:n.-1044G>C