Canonical Allele Identifier: CA581667416
Gene: MCM4 HGNC NCBI

Linked Data

gnomAD v2: 8-48872786-T-C
gnomAD v4: 8-47960226-T-C
MyVariant Identifiers: chr8:g.48872786T>C (hg19) chr8:g.47960226T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960226T>C , CM000670.2:g.47960226T>C GRCh38
NC_000008.10:g.48872786T>C , CM000670.1:g.48872786T>C GRCh37
NC_000008.9:g.49035339T>C NCBI36
NG_023435.1:g.4958A>G , LRG_162:g.4958A>G
NG_032967.1:g.5024T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-109T>C ENSP00000430329.1:n.-109T>C
NM_005914.3:c.-919T>C NP_005905.2:n.-919T>C
NM_182746.2:c.-803T>C NP_877423.1:n.-803T>C
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