Canonical Allele Identifier: CA852595291
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1356646257
gnomAD v3: 8-47960230-G-C
gnomAD v4: 8-47960230-G-C
MyVariant Identifiers: chr8:g.48872790G>C (hg19) chr8:g.47960230G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960230G>C , CM000670.2:g.47960230G>C GRCh38
NC_000008.10:g.48872790G>C , CM000670.1:g.48872790G>C GRCh37
NC_000008.9:g.49035343G>C NCBI36
NG_023435.1:g.4954C>G , LRG_162:g.4954C>G
NG_032967.1:g.5028G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-105G>C ENSP00000430329.1:n.-105G>C
NM_005914.3:c.-915G>C NP_005905.2:n.-915G>C
NM_182746.2:c.-799G>C NP_877423.1:n.-799G>C
Search 100 bp 5'
Search 100 bp 3'