Canonical Allele Identifier: CA852595491
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1296912136
gnomAD v3: 8-47960441-G-A
gnomAD v4: 8-47960441-G-A
MyVariant Identifiers: chr8:g.48873001G>A (hg19) chr8:g.47960441G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960441G>A , CM000670.2:g.47960441G>A GRCh38
NC_000008.10:g.48873001G>A , CM000670.1:g.48873001G>A GRCh37
NC_000008.9:g.49035554G>A NCBI36
NG_023435.1:g.4743C>T , LRG_162:g.4743C>T
NG_032967.1:g.5239G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+121G>A ENSP00000430329.1:n.-15+121G>A
NM_005914.3:c.-704G>A NP_005905.2:n.-704G>A
NM_182746.2:c.-588G>A NP_877423.1:n.-588G>A
XM_005251234.1:c.-950G>A XP_005251291.1:n.-950G>A
Search 100 bp 5'
Search 100 bp 3'