Canonical Allele Identifier: CA2687209801
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960467-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960467A>T , CM000670.2:g.47960467A>T GRCh38
NC_000008.10:g.48873027A>T , CM000670.1:g.48873027A>T GRCh37
NC_000008.9:g.49035580A>T NCBI36
NG_023435.1:g.4717T>A , LRG_162:g.4717T>A
NG_032967.1:g.5265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+147A>T ENSP00000430329.1:n.-15+147A>T
NM_005914.3:c.-678A>T NP_005905.2:n.-678A>T
NM_182746.2:c.-562A>T NP_877423.1:n.-562A>T
XM_005251234.1:c.-924A>T XP_005251291.1:n.-924A>T