Canonical Allele Identifier: CA581667445
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1319375779
gnomAD v2: 8-48872905-T-G
gnomAD v3: 8-47960345-T-G
gnomAD v4: 8-47960345-T-G
MyVariant Identifiers: chr8:g.48872905T>G (hg19) chr8:g.47960345T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960345T>G , CM000670.2:g.47960345T>G GRCh38
NC_000008.10:g.48872905T>G , CM000670.1:g.48872905T>G GRCh37
NC_000008.9:g.49035458T>G NCBI36
NG_023435.1:g.4839A>C , LRG_162:g.4839A>C
NG_032967.1:g.5143T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+25T>G ENSP00000430329.1:n.-15+25T>G
NM_005914.3:c.-800T>G NP_005905.2:n.-800T>G
NM_182746.2:c.-684T>G NP_877423.1:n.-684T>G
XM_005251234.1:c.-1046T>G XP_005251291.1:n.-1046T>G
Search 100 bp 5'
Search 100 bp 3'