Canonical Allele Identifier: CA2687209559
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v4: 8-47960296-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960296A>C , CM000670.2:g.47960296A>C GRCh38
NC_000008.10:g.48872856A>C , CM000670.1:g.48872856A>C GRCh37
NC_000008.9:g.49035409A>C NCBI36
NG_023435.1:g.4888T>G , LRG_162:g.4888T>G
NG_032967.1:g.5094A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-39A>C ENSP00000430329.1:n.-39A>C
NM_005914.3:c.-849A>C NP_005905.2:n.-849A>C
NM_182746.2:c.-733A>C NP_877423.1:n.-733A>C
XM_005251234.1:c.-1095A>C XP_005251291.1:n.-1095A>C
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