Canonical Allele Identifier: CA176153938
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs968693074
gnomAD v3: 8-47960261-G-A
gnomAD v4: 8-47960261-G-A
MyVariant Identifiers: chr8:g.48872821G>A (hg19) chr8:g.47960261G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960261G>A , CM000670.2:g.47960261G>A GRCh38
NC_000008.10:g.48872821G>A , CM000670.1:g.48872821G>A GRCh37
NC_000008.9:g.49035374G>A NCBI36
NG_023435.1:g.4923C>T , LRG_162:g.4923C>T
NG_032967.1:g.5059G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-74G>A ENSP00000430329.1:n.-74G>A
NM_005914.3:c.-884G>A NP_005905.2:n.-884G>A
NM_182746.2:c.-768G>A NP_877423.1:n.-768G>A
XM_005251234.1:c.-1130G>A XP_005251291.1:n.-1130G>A
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