Canonical Allele Identifier: CA2717398831
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2154504885
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960256A>T , CM000670.2:g.47960256A>T GRCh38
NC_000008.10:g.48872816A>T , CM000670.1:g.48872816A>T GRCh37
NC_000008.9:g.49035369A>T NCBI36
NG_023435.1:g.4928T>A , LRG_162:g.4928T>A
NG_032967.1:g.5054A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-79A>T ENSP00000430329.1:n.-79A>T
NM_005914.3:c.-889A>T NP_005905.2:n.-889A>T
NM_182746.2:c.-773A>T NP_877423.1:n.-773A>T
XM_005251234.1:c.-1135A>T XP_005251291.1:n.-1135A>T
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