Canonical Allele Identifier: CA176153967
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs771934701
gnomAD v4: 8-47960293-C-T
MyVariant Identifiers: chr8:g.48872853C>T (hg19) chr8:g.47960293C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960293C>T , CM000670.2:g.47960293C>T GRCh38
NC_000008.10:g.48872853C>T , CM000670.1:g.48872853C>T GRCh37
NC_000008.9:g.49035406C>T NCBI36
NG_023435.1:g.4891G>A , LRG_162:g.4891G>A
NG_032967.1:g.5091C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-42C>T ENSP00000430329.1:n.-42C>T
NM_005914.3:c.-852C>T NP_005905.2:n.-852C>T
NM_182746.2:c.-736C>T NP_877423.1:n.-736C>T
XM_005251234.1:c.-1098C>T XP_005251291.1:n.-1098C>T
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