Canonical Allele Identifier: CA2687209506
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2154504886
gnomAD v4: 8-47960272-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960272T>G , CM000670.2:g.47960272T>G GRCh38
NC_000008.10:g.48872832T>G , CM000670.1:g.48872832T>G GRCh37
NC_000008.9:g.49035385T>G NCBI36
NG_023435.1:g.4912A>C , LRG_162:g.4912A>C
NG_032967.1:g.5070T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-63T>G ENSP00000430329.1:n.-63T>G
NM_005914.3:c.-873T>G NP_005905.2:n.-873T>G
NM_182746.2:c.-757T>G NP_877423.1:n.-757T>G
XM_005251234.1:c.-1119T>G XP_005251291.1:n.-1119T>G
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