Canonical Allele Identifier: CA852595399
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1288993568
MyVariant Identifiers: chr8:g.48872928G>C (hg19) chr8:g.47960368G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960368G>C , CM000670.2:g.47960368G>C GRCh38
NC_000008.10:g.48872928G>C , CM000670.1:g.48872928G>C GRCh37
NC_000008.9:g.49035481G>C NCBI36
NG_023435.1:g.4816C>G , LRG_162:g.4816C>G
NG_032967.1:g.5166G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+48G>C ENSP00000430329.1:n.-15+48G>C
NM_005914.3:c.-777G>C NP_005905.2:n.-777G>C
NM_182746.2:c.-661G>C NP_877423.1:n.-661G>C
XM_005251234.1:c.-1023G>C XP_005251291.1:n.-1023G>C
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