Canonical Allele Identifier: CA852595288
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1443131218
MyVariant Identifiers: chr8:g.48872779G>C (hg19) chr8:g.47960219G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960219G>C , CM000670.2:g.47960219G>C GRCh38
NC_000008.10:g.48872779G>C , CM000670.1:g.48872779G>C GRCh37
NC_000008.9:g.49035332G>C NCBI36
NG_023435.1:g.4965C>G , LRG_162:g.4965C>G
NG_032967.1:g.5017G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-116G>C ENSP00000430329.1:n.-116G>C
NM_005914.3:c.-926G>C NP_005905.2:n.-926G>C
NM_182746.2:c.-810G>C NP_877423.1:n.-810G>C
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