Canonical Allele Identifier: CA2687209498
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960270-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960270T>C , CM000670.2:g.47960270T>C GRCh38
NC_000008.10:g.48872830T>C , CM000670.1:g.48872830T>C GRCh37
NC_000008.9:g.49035383T>C NCBI36
NG_023435.1:g.4914A>G , LRG_162:g.4914A>G
NG_032967.1:g.5068T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-65T>C ENSP00000430329.1:n.-65T>C
NM_005914.3:c.-875T>C NP_005905.2:n.-875T>C
NM_182746.2:c.-759T>C NP_877423.1:n.-759T>C
XM_005251234.1:c.-1121T>C XP_005251291.1:n.-1121T>C