Canonical Allele Identifier: CA581667449
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs997930929
gnomAD v2: 8-48872915-T-C
gnomAD v3: 8-47960355-T-C
gnomAD v4: 8-47960355-T-C
MyVariant Identifiers: chr8:g.48872915T>C (hg19) chr8:g.47960355T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960355T>C , CM000670.2:g.47960355T>C GRCh38
NC_000008.10:g.48872915T>C , CM000670.1:g.48872915T>C GRCh37
NC_000008.9:g.49035468T>C NCBI36
NG_023435.1:g.4829A>G , LRG_162:g.4829A>G
NG_032967.1:g.5153T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+35T>C ENSP00000430329.1:n.-15+35T>C
NM_005914.3:c.-790T>C NP_005905.2:n.-790T>C
NM_182746.2:c.-674T>C NP_877423.1:n.-674T>C
XM_005251234.1:c.-1036T>C XP_005251291.1:n.-1036T>C
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