Canonical Allele Identifier: CA176154006
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1022017845
gnomAD v2: 8-48872950-G-A
gnomAD v3: 8-47960390-G-A
gnomAD v4: 8-47960390-G-A
MyVariant Identifiers: chr8:g.48872950G>A (hg19) chr8:g.47960390G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960390G>A , CM000670.2:g.47960390G>A GRCh38
NC_000008.10:g.48872950G>A , CM000670.1:g.48872950G>A GRCh37
NC_000008.9:g.49035503G>A NCBI36
NG_023435.1:g.4794C>T , LRG_162:g.4794C>T
NG_032967.1:g.5188G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+70G>A ENSP00000430329.1:n.-15+70G>A
NM_005914.3:c.-755G>A NP_005905.2:n.-755G>A
NM_182746.2:c.-639G>A NP_877423.1:n.-639G>A
XM_005251234.1:c.-1001G>A XP_005251291.1:n.-1001G>A
Search 100 bp 5'
Search 100 bp 3'