Canonical Allele Identifier: CA581667467
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1167060851
gnomAD v2: 8-48873025-G-T
gnomAD v3: 8-47960465-G-T
gnomAD v4: 8-47960465-G-T
MyVariant Identifiers: chr8:g.48873025G>T (hg19) chr8:g.47960465G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960465G>T , CM000670.2:g.47960465G>T GRCh38
NC_000008.10:g.48873025G>T , CM000670.1:g.48873025G>T GRCh37
NC_000008.9:g.49035578G>T NCBI36
NG_023435.1:g.4719C>A , LRG_162:g.4719C>A
NG_032967.1:g.5263G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+145G>T ENSP00000430329.1:n.-15+145G>T
NM_005914.3:c.-680G>T NP_005905.2:n.-680G>T
NM_182746.2:c.-564G>T NP_877423.1:n.-564G>T
XM_005251234.1:c.-926G>T XP_005251291.1:n.-926G>T
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